Multi-event July 2018 FDA Recall Drug by King Bio Inc.

This Multi-event Class I drug recall was voluntarily initiated by King Bio Inc. on July 20, 2018 for the product Drug. The FDA reported the reason for recall as microbial contamination. The product was distributed Nationwide and the recall is currently terminated.

Reported Recall Events

D-0718-2019 TERMINATED D-0767-2019 TERMINATED D-0829-2019 TERMINATED D-0836-2019 TERMINATED D-0599-2019 TERMINATED D-0794-2019 TERMINATED D-0537-2019 TERMINATED D-0837-2019 TERMINATED D-0974-2019 TERMINATED D-0664-2019 TERMINATED D-0594-2019 TERMINATED D-0833-2019 TERMINATED D-0577-2019 TERMINATED D-0927-2019 TERMINATED D-0715-2019 TERMINATED D-0588-2019 TERMINATED D-0779-2019 TERMINATED D-0847-2019 TERMINATED D-0616-2019 TERMINATED D-0820-2019 TERMINATED D-0946-2019 TERMINATED D-0759-2019 TERMINATED D-0962-2019 TERMINATED D-0612-2019 TERMINATED D-0691-2019 TERMINATED D-0696-2019 TERMINATED D-0808-2019 TERMINATED D-0579-2019 TERMINATED D-0593-2019 TERMINATED D-0786-2019 TERMINATED D-0747-2019 TERMINATED D-0812-2019 TERMINATED D-0591-2019 TERMINATED D-0966-2019 TERMINATED D-0707-2019 TERMINATED D-0856-2019 TERMINATED D-0884-2019 TERMINATED D-0882-2019 TERMINATED D-0662-2019 TERMINATED D-0719-2019 TERMINATED D-0827-2019 TERMINATED D-0692-2019 TERMINATED D-0703-2019 TERMINATED D-0795-2019 TERMINATED D-0893-2019 TERMINATED D-0803-2019 TERMINATED D-0558-2019 TERMINATED D-0573-2019 TERMINATED D-0608-2019 TERMINATED D-0944-2019 TERMINATED D-0529-2019 TERMINATED D-0923-2019 TERMINATED D-0951-2019 TERMINATED D-0920-2019 TERMINATED D-0609-2019 TERMINATED D-0745-2019 TERMINATED D-0934-2019 TERMINATED D-0736-2019 TERMINATED D-0583-2019 TERMINATED D-0816-2019 TERMINATED D-0706-2019 TERMINATED D-0760-2019 TERMINATED D-0853-2019 TERMINATED D-0906-2019 TERMINATED D-0626-2019 TERMINATED D-0874-2019 TERMINATED D-0917-2019 TERMINATED D-0822-2019 TERMINATED D-0635-2019 TERMINATED D-0965-2019 TERMINATED D-0628-2019 TERMINATED D-0722-2019 TERMINATED D-0525-2019 TERMINATED D-0532-2019 TERMINATED D-0850-2019 TERMINATED D-0643-2019 TERMINATED D-0830-2019 TERMINATED D-0910-2019 TERMINATED D-0866-2019 TERMINATED D-0926-2019 TERMINATED D-0649-2019 TERMINATED D-0734-2019 TERMINATED D-0683-2019 TERMINATED D-0867-2019 TERMINATED D-0676-2019 TERMINATED D-0978-2019 TERMINATED D-0523-2019 TERMINATED D-0567-2019 TERMINATED D-0849-2019 TERMINATED D-0666-2019 TERMINATED D-0548-2019 TERMINATED D-0641-2019 TERMINATED D-0533-2019 TERMINATED D-0637-2019 TERMINATED D-0855-2019 TERMINATED D-0825-2019 TERMINATED D-0975-2019 TERMINATED D-0790-2019 TERMINATED D-0981-2019 TERMINATED D-0768-2019 TERMINATED D-0840-2019 TERMINATED D-0695-2019 TERMINATED D-0961-2019 TERMINATED D-0665-2019 TERMINATED D-0755-2019 TERMINATED D-0563-2019 TERMINATED D-0774-2019 TERMINATED D-0957-2019 TERMINATED D-0885-2019 TERMINATED D-0839-2019 TERMINATED D-0739-2019 TERMINATED D-0544-2019 TERMINATED D-0782-2019 TERMINATED D-0655-2019 TERMINATED D-0688-2019 TERMINATED D-0653-2019 TERMINATED D-0710-2019 TERMINATED D-0648-2019 TERMINATED D-0781-2019 TERMINATED D-0757-2019 TERMINATED D-0933-2019 TERMINATED D-0601-2019 TERMINATED D-0619-2019 TERMINATED D-0551-2019 TERMINATED D-0737-2019 TERMINATED D-0694-2019 TERMINATED D-0671-2019 TERMINATED D-0726-2019 TERMINATED D-0809-2019 TERMINATED D-0661-2019 TERMINATED D-0733-2019 TERMINATED D-0743-2019 TERMINATED D-0780-2019 TERMINATED D-0971-2019 TERMINATED D-0720-2019 TERMINATED D-0566-2019 TERMINATED D-0754-2019 TERMINATED D-0576-2019 TERMINATED D-0878-2019 TERMINATED D-0574-2019 TERMINATED D-0670-2019 TERMINATED D-0526-2019 TERMINATED D-0887-2019 TERMINATED D-0824-2019 TERMINATED D-0678-2019 TERMINATED D-0924-2019 TERMINATED D-0791-2019 TERMINATED D-0697-2019 TERMINATED D-0773-2019 TERMINATED D-0689-2019 TERMINATED D-0778-2019 TERMINATED D-0956-2019 TERMINATED D-0793-2019 TERMINATED D-0969-2019 TERMINATED D-0679-2019 TERMINATED D-0702-2019 TERMINATED D-0629-2019 TERMINATED D-0541-2019 TERMINATED D-0811-2019 TERMINATED D-0547-2019 TERMINATED D-0783-2019 TERMINATED D-0896-2019 TERMINATED D-0610-2019 TERMINATED D-0845-2019 TERMINATED D-0656-2019 TERMINATED D-0611-2019 TERMINATED D-0620-2019 TERMINATED D-0568-2019 TERMINATED D-0581-2019 TERMINATED D-0521-2019 TERMINATED D-0729-2019 TERMINATED D-0746-2019 TERMINATED D-0553-2019 TERMINATED D-0819-2019 TERMINATED D-0938-2019 TERMINATED D-0806-2019 TERMINATED D-0687-2019 TERMINATED D-0913-2019 TERMINATED D-0613-2019 TERMINATED D-0848-2019 TERMINATED D-0598-2019 TERMINATED D-0693-2019 TERMINATED D-0642-2019 TERMINATED D-0835-2019 TERMINATED D-0868-2019 TERMINATED D-0716-2019 TERMINATED D-0549-2019 TERMINATED D-0538-2019 TERMINATED D-0976-2019 TERMINATED D-0669-2019 TERMINATED D-0980-2019 TERMINATED D-0817-2019 TERMINATED D-0950-2019 TERMINATED D-0912-2019 TERMINATED D-0818-2019 TERMINATED D-0796-2019 TERMINATED D-0578-2019 TERMINATED D-0901-2019 TERMINATED D-0982-2019 TERMINATED D-0919-2019 TERMINATED D-0554-2019 TERMINATED D-0915-2019 TERMINATED D-0959-2019 TERMINATED D-0799-2019 TERMINATED D-0797-2019 TERMINATED D-0918-2019 TERMINATED D-0929-2019 TERMINATED D-0622-2019 TERMINATED D-0751-2019 TERMINATED D-0888-2019 TERMINATED D-0921-2019 TERMINATED D-0769-2019 TERMINATED D-0851-2019 TERMINATED D-0606-2019 TERMINATED D-0527-2019 TERMINATED D-0582-2019 TERMINATED D-0546-2019 TERMINATED D-0708-2019 TERMINATED D-0663-2019 TERMINATED D-0789-2019 TERMINATED D-0823-2019 TERMINATED D-0869-2019 TERMINATED D-0630-2019 TERMINATED D-0939-2019 TERMINATED D-0586-2019 TERMINATED D-0844-2019 TERMINATED D-0954-2019 TERMINATED D-0940-2019 TERMINATED D-0930-2019 TERMINATED D-0559-2019 TERMINATED D-0603-2019 TERMINATED D-0698-2019 TERMINATED D-0651-2019 TERMINATED D-0714-2019 TERMINATED D-0704-2019 TERMINATED D-0828-2019 TERMINATED D-0740-2019 TERMINATED D-0771-2019 TERMINATED D-0788-2019 TERMINATED D-0724-2019 TERMINATED D-0936-2019 TERMINATED D-0960-2019 TERMINATED D-0947-2019 TERMINATED D-0530-2019 TERMINATED D-0592-2019 TERMINATED D-0540-2019 TERMINATED D-0846-2019 TERMINATED D-0815-2019 TERMINATED D-0727-2019 TERMINATED D-0907-2019 TERMINATED D-0897-2019 TERMINATED D-0948-2019 TERMINATED D-0605-2019 TERMINATED D-0843-2019 TERMINATED D-0750-2019 TERMINATED D-0838-2019 TERMINATED D-0864-2019 TERMINATED D-0832-2019 TERMINATED D-0652-2019 TERMINATED D-0859-2019 TERMINATED D-0677-2019 TERMINATED D-0890-2019 TERMINATED D-0928-2019 TERMINATED D-0550-2019 TERMINATED D-0772-2019 TERMINATED D-0561-2019 TERMINATED D-0770-2019 TERMINATED D-0953-2019 TERMINATED D-0657-2019 TERMINATED D-0862-2019 TERMINATED D-0762-2019 TERMINATED D-0784-2019 TERMINATED D-0735-2019 TERMINATED D-0638-2019 TERMINATED D-0802-2019 TERMINATED D-0672-2019 TERMINATED D-0623-2019 TERMINATED D-0925-2019 TERMINATED D-0589-2019 TERMINATED D-0860-2019 TERMINATED D-0826-2019 TERMINATED D-0942-2019 TERMINATED D-0880-2019 TERMINATED D-0922-2019 TERMINATED D-0684-2019 TERMINATED D-0800-2019 TERMINATED D-0712-2019 TERMINATED D-0973-2019 TERMINATED D-0536-2019 TERMINATED D-0522-2019 TERMINATED D-0753-2019 TERMINATED D-0967-2019 TERMINATED D-0711-2019 TERMINATED D-0858-2019 TERMINATED D-0700-2019 TERMINATED D-0633-2019 TERMINATED D-0627-2019 TERMINATED D-0865-2019 TERMINATED D-0841-2019 TERMINATED D-0690-2019 TERMINATED D-0650-2019 TERMINATED D-0528-2019 TERMINATED D-0877-2019 TERMINATED D-0680-2019 TERMINATED D-0985-2019 TERMINATED D-0776-2019 TERMINATED D-0834-2019 TERMINATED D-0875-2019 TERMINATED D-0667-2019 TERMINATED D-0660-2019 TERMINATED D-0646-2019 TERMINATED D-0758-2019 TERMINATED D-0748-2019 TERMINATED D-0552-2019 TERMINATED D-0945-2019 TERMINATED D-0713-2019 TERMINATED D-0564-2019 TERMINATED D-0763-2019 TERMINATED D-0984-2019 TERMINATED D-0842-2019 TERMINATED D-0861-2019 TERMINATED D-0792-2019 TERMINATED D-0614-2019 TERMINATED D-0659-2019 TERMINATED D-0560-2019 TERMINATED D-0798-2019 TERMINATED D-0542-2019 TERMINATED D-0604-2019 TERMINATED D-0681-2019 TERMINATED D-0699-2019 TERMINATED D-0640-2019 TERMINATED D-0952-2019 TERMINATED D-0881-2019 TERMINATED D-0879-2019 TERMINATED D-0556-2019 TERMINATED D-0721-2019 TERMINATED D-0775-2019 TERMINATED D-0658-2019 TERMINATED D-0617-2019 TERMINATED D-0904-2019 TERMINATED D-0565-2019 TERMINATED D-0886-2019 TERMINATED D-0738-2019 TERMINATED D-0898-2019 TERMINATED D-0909-2019 TERMINATED D-0955-2019 TERMINATED D-0744-2019 TERMINATED D-0831-2019 TERMINATED D-0632-2019 TERMINATED D-0572-2019 TERMINATED D-0562-2019 TERMINATED D-0963-2019 TERMINATED D-0682-2019 TERMINATED D-0673-2019 TERMINATED D-0804-2019 TERMINATED D-0979-2019 TERMINATED D-0900-2019 TERMINATED D-0814-2019 TERMINATED D-0686-2019 TERMINATED D-0725-2019 TERMINATED D-0597-2019 TERMINATED D-0668-2019 TERMINATED D-0968-2019 TERMINATED D-0723-2019 TERMINATED D-0941-2019 TERMINATED D-0807-2019 TERMINATED D-0587-2019 TERMINATED D-0675-2019 TERMINATED D-0894-2019 TERMINATED D-0854-2019 TERMINATED D-0585-2019 TERMINATED D-0645-2019 TERMINATED D-0872-2019 TERMINATED D-0543-2019 TERMINATED D-0931-2019 TERMINATED D-0631-2019 TERMINATED D-0801-2019 TERMINATED D-0569-2019 TERMINATED D-0805-2019 TERMINATED D-0644-2019 TERMINATED D-0916-2019 TERMINATED D-0701-2019 TERMINATED D-0584-2019 TERMINATED D-0813-2019 TERMINATED D-0766-2019 TERMINATED D-0709-2019 TERMINATED D-0539-2019 TERMINATED D-0607-2019 TERMINATED D-0983-2019 TERMINATED D-0871-2019 TERMINATED D-0600-2019 TERMINATED D-0639-2019 TERMINATED D-0545-2019 TERMINATED D-0602-2019 TERMINATED D-0977-2019 TERMINATED D-0685-2019 TERMINATED D-0731-2019 TERMINATED D-0852-2019 TERMINATED D-0557-2019 TERMINATED D-0535-2019 TERMINATED D-0571-2019 TERMINATED D-0531-2019 TERMINATED D-0575-2019 TERMINATED D-0911-2019 TERMINATED D-0524-2019 TERMINATED D-0647-2019 TERMINATED D-0752-2019 TERMINATED D-0624-2019 TERMINATED D-0756-2019 TERMINATED D-0596-2019 TERMINATED D-0870-2019 TERMINATED D-0972-2019 TERMINATED D-0777-2019 TERMINATED D-0903-2019 TERMINATED D-0615-2019 TERMINATED D-0674-2019 TERMINATED D-0595-2019 TERMINATED D-0895-2019 TERMINATED D-0749-2019 TERMINATED D-0970-2019 TERMINATED D-0590-2019 TERMINATED D-0932-2019 TERMINATED D-0732-2019 TERMINATED D-0908-2019 TERMINATED D-0618-2019 TERMINATED D-0534-2019 TERMINATED D-0741-2019 TERMINATED D-0949-2019 TERMINATED D-0964-2019 TERMINATED D-0889-2019 TERMINATED D-0570-2019 TERMINATED D-0821-2019 TERMINATED D-0705-2019 TERMINATED D-0654-2019 TERMINATED D-0625-2019 TERMINATED D-0761-2019 TERMINATED D-0905-2019 TERMINATED D-0914-2019 TERMINATED D-0899-2019 TERMINATED D-0863-2019 TERMINATED D-0580-2019 TERMINATED D-0787-2019 TERMINATED D-0935-2019 TERMINATED D-0892-2019 TERMINATED D-0958-2019 TERMINATED D-0765-2019 TERMINATED D-0636-2019 TERMINATED D-0876-2019 TERMINATED D-0728-2019 TERMINATED D-0717-2019 TERMINATED D-0730-2019 TERMINATED D-0891-2019 TERMINATED D-0742-2019 TERMINATED D-0555-2019 TERMINATED D-0943-2019 TERMINATED D-0634-2019 TERMINATED D-0764-2019 TERMINATED D-0873-2019 TERMINATED D-0810-2019 TERMINATED D-0857-2019 TERMINATED D-0902-2019 TERMINATED D-0883-2019 TERMINATED D-0785-2019 TERMINATED D-0621-2019 TERMINATED D-0937-2019 TERMINATED

Recall Number: D-0718-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
92 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx M3 Metabolic Mineral Modulator, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955027621, NDC 57955-0277-2

Batch or Lot Expiration Information

Lot# Lots: 022216B Exp. 02/19; 062216S Exp. 06/19; 011217B Exp. 01/20

Recall Number: D-0767-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
789 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Arthritis & Joint Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955016229, NDC 57955-0162-2

Batch or Lot Expiration Information

Lot# Lots: 091015M Exp. 09/18; 022317D Exp. 02/20

Recall Number: D-0829-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
586 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Aller-Detox: Herbicides & Pesticides, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955240624, NDC 57955-2406-2

Batch or Lot Expiration Information

Lot# Lots: 072115D Exp. 07/18; 060216B Exp. 06/19

Recall Number: D-0836-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
10 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Religious Issues, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955254027, NDC 57955-2541-2

Batch or Lot Expiration Information

Lot# Lot: 063016B Exp. 06/19

Recall Number: D-0599-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1469 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic ShinglePlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 35795551829, NDC 57955-5518-2

Batch or Lot Expiration Information

Lot# Lots: 081815L Exp. 08/18; 010118Q Exp. 01/2020; 050216Z Exp. 05/19; 120616E Exp. 12/19

Recall Number: D-0794-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
995 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Bactero Reliever, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955011729, NDC 57955-0117-2

Batch or Lot Expiration Information

Lot# Lots: 092915F Exp. 09/18; 081616B Exp. 08/19; 041416A Exp. 04/19

Recall Number: D-0537-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4374 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Migraine Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955502821, NDC 57955-5028-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 011617D Exp. 01/20; 030818M Exp. 03/20; 083116B Exp. 08/2019; 101217B Exp. 10/19

Recall Number: D-0837-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
230 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Hair & Nails Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955004929, NDC 57955-0049-2

Batch or Lot Expiration Information

Lot# Lots: 072015F Exp. 07/18; 062816E Exp. 06/19; 100316E Exp. 10/19

Recall Number: D-0974-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
988 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Sinus Relief High Potency Homeopathic Formula, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955013426, NDC 57955-0134-2

Batch or Lot Expiration Information

Lot# Lots: 120816J Exp. 12/19; 123115C Exp. 12/18

Recall Number: D-0664-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1010 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine for kids! Children's Cough Relief Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955514527, NDC 57955-6145-2

Batch or Lot Expiration Information

Lot# Lots: 021216J Exp. 02/2019; 030916T Exp. 03/2019; 092815E Exp. 09/2018

Recall Number: D-0594-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
5170 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Stress Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955507925, NDC 57955-5852-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 012616B Exp. 01/19; 020817E Exp. 02/20; 071818G Exp. 07/20; 111017C Exp. 11/19

Recall Number: D-0833-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
23 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Odor Freee..., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955013020, NDC 57955-0130-2

Batch or Lot Expiration Information

Lot# Lots: 052516G Exp. 05/19

Recall Number: D-0577-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
975 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Blood & Kidney Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955506126, NDC 57955-5061-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 010517C Exp. 01/20; 050216D Exp. 05/19

Recall Number: D-0927-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
403 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #10 (Maroon Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-020118H Exp. 02/20; AUS-102617A Exp. 10/19

Recall Number: D-0715-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
549 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx ICV Clenz Cleansing & Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955009825, NDC 57955-0262-2

Batch or Lot Expiration Information

Lot# Lots: 081015G Exp. 08/18; 030916B Exp. 03/19; 012317B Exp. 01/20; 010818A Exp. 01/20

Recall Number: D-0588-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4191 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Wart Freee, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955505921, NDC 57955-5059-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 010518F Exp. 01/20; 011416A Exp. 01/19; 072216J Exp. 07/19; 100417B Exp. 10/19; 123115B Exp. 12/18

Recall Number: D-0779-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
24 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Self-Pity, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955253020, NDC 57955-2532-2

Batch or Lot Expiration Information

Lot# Lots: 031016G Exp. 03/19; 081916B Exp. 08/19

Recall Number: D-0847-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1229 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx First Aid for Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955177029, NDC 57955-1770-2

Batch or Lot Expiration Information

Lot# Lots: 072815Q Exp. 07/18; 081815E Exp. 08/18; 091216F Exp. 09/19; 071317A Exp. 07/19

Recall Number: D-0616-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
606 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Female Libido, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955511526, NDC 57955-5515-2

Batch or Lot Expiration Information

Lot# Lots: 020618E Exp. 02/20; 080916U Exp. 08/18; 102816C Exp. 10/19

Recall Number: D-0820-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
102 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Eye Stress, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955015123, NDC 57955-0151-2

Batch or Lot Expiration Information

Lot# Lots: 060616E Exp. 06/19; 121317F Exp. 12/19

Recall Number: D-0946-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
9888 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #7 Flora Plus Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4207-2

Batch or Lot Expiration Information

Lot# Lots: NR-090115K Exp. 09/18; NR-031516G Exp. 03/19; NR-011216E Exp. 10/19; NR-021717D Exp. 02/20; NR-042717C Exp. 04/20; NR-061616F Exp. 06/19; NR-090616F Exp. 09/19; NR-101416G Exp. 10/19; NR-120815M Exp. 12/18; NR-020118H Exp. 02/20; NR-020618J Exp. 02/20; NR-081017H Exp. 08/19; NR-101117E Exp. 10/19

Recall Number: D-0759-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
500 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Bladder Formula Urinary, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955004523, NDC 57955-0094-2

Batch or Lot Expiration Information

Lot# Lots: 072815K Exp. 07/18; 080916F Exp. 08/19; 022117F Exp. 02/20; 052616P Exp. 05/19

Recall Number: D-0962-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
10418 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Aquaflora Candida High Potency 9 Multi-Strain Candida Formula, 236 mL, (liquid/liquide), Manufactured by:/Fabrique par: King Bio, Inc. 3 Westside Dr., Asheville, NC 28805 USA Import by: Importe par: Ambiental Solutions Inc. Vancouver, BC, V5Y 1E6, DIN-HM 80036805 UPC 357955180289

Batch or Lot Expiration Information

Lot# Lots: 022218E Exp. 02/20; 011217C Exp. 12/20; 012116A Exp. 01/19; 092816A Exp. 09/19

Recall Number: D-0612-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
388 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Fragrance & Phenolic Allergy Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955520023, NDC 57955-6136-2

Batch or Lot Expiration Information

Lot# Lots: 012616F Exp. 01/19; 081315F Exp. 08/18; 010418L Exp. 01/20

Recall Number: D-0691-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
6 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Children's Appetite Enhancer Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955031826, NDC 57955-0318-2

Batch or Lot Expiration Information

Lot# Lots: 022316G Exp. 02/19

Recall Number: D-0696-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
12280 tubes

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Cooling Acute Pain Relief Pure Homeopathic Cream, 3 oz. (85 g), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955400134, NDC 57955-4001-3

Batch or Lot Expiration Information

Lot# Lots: 060816 Exp. 06/19; 081717ZZ Exp. 08/19; 110117ZZ Exp. 11/20; 045017ZZ Exp. 04/20; 100516ZZ Exp. 06/19; 111016ZZ Exp. 11/19

Recall Number: D-0808-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
70 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Insecurity, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955256021, NDC 57955-2561-2

Batch or Lot Expiration Information

Lot# Lots: 042116A Exp. 04/19; 072216N Exp. 07/19

Recall Number: D-0579-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
328 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Dairy Intolerances, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955519829, NDC 57955-6722-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 042116B Exp. 04/19; 062416A Exp. 06/19

Recall Number: D-0593-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
282 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Stye Relief, 2 fl. oz. (59 mL),King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955512523, NDC 57955-5125-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 020618F Exp. 02/20; 052516AA Exp. 05/19; 091516E Exp. 09/19

Recall Number: D-0786-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
245 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Gout Symptom Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955002123, NDC 57955-0021-2

Batch or Lot Expiration Information

Lot# Lots: 091216G Exp. 09/19; 032216F Exp. 03/19

Recall Number: D-0747-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
41 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Alcoholism Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955302025, NDC 57955-3021-2

Batch or Lot Expiration Information

Lot# Lot: 021217A Exp. 02/20

Recall Number: D-0812-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
13 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Personality Changes, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955105022, NDC 57955-1053-2

Batch or Lot Expiration Information

Lot# Lot: 051716F Exp. 05/19

Recall Number: D-0591-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2225 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Teeth & Gums Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955507321, NDC 57955-5073-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 010517E Exp. 01/20; 010518A Exp. 01/20; 022417C Exp. 02/20; 052516H Exp. 05/19; 091616D Exp. 09/19; 112016A Exp. 11/19

Recall Number: D-0966-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
710 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Regional Allergies Canadian Prairies, 59 mL (liquid/liquide), DIN-HM 80074815 UPC 357955181729

Batch or Lot Expiration Information

Lot# Lot: 021517L Exp. 02/20

Recall Number: D-0707-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1621 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies Southwest U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955175025, NDC 57955-2715-2

Batch or Lot Expiration Information

Lot# Lots: 030818A Exp. 03/20; 011416B Exp. 01/19; 111016B Exp. 11/19

Recall Number: D-0856-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
144 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx ChemoClenz, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955007128, NDC 57955-0071-2

Batch or Lot Expiration Information

Lot# Lots: 062415G Exp. 06/18; 080916X Exp. 08/19

Recall Number: D-0884-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
61 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies: Fruits & Vegetables, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955250128, NDC 57955-2501-2

Batch or Lot Expiration Information

Lot# Lots: 112117E Exp. 11/19; 091216B Exp. 09/19

Recall Number: D-0882-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
388 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Restless Mind, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955153023, NDC 57955-1531-2

Batch or Lot Expiration Information

Lot# Lots: 091415A Exp. 09/18; 113015K Exp. 11/18; 122915A Exp. 12/18

Recall Number: D-0662-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
257 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Baby Colic Relief Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955515821, NDC 57955-0466-2

Batch or Lot Expiration Information

Lot# Lots: 020118H Exp. 02/2020; 092017A Exp. 09/2019

Recall Number: D-0719-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
217 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx GallPlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006824, NDC 57955-0340-2

Batch or Lot Expiration Information

Lot# Lots: 110916A Exp. 11/19; 011518B Exp. 01/20

Recall Number: D-0827-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
143 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Restless Leg Syndrome, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955044529, NDC 57955-0445-2

Batch or Lot Expiration Information

Lot# Lots: 051716X Exp. 05/19; 101116A Exp. 10/19

Recall Number: D-0692-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
223 tubes

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Warming Arthritic Pain & Joint Relief Homeopathic Cream, Net Wt. 3 oz. (85 g), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955093534, NDC 57955-0935-3

Batch or Lot Expiration Information

Lot# Lots: 020318ZZ Exp. 02/20; 051418ZZ Exp. 05/20; 060118ZZ Exp. 06/20; 020418ZZ Exp. 02/20; 020518ZZ Exp. 02/20

Recall Number: D-0703-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
335 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Wart Freee..., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955005926, NDC 57955-0360-2

Batch or Lot Expiration Information

Lot# Lots: 060816B Exp. 06/19; 012017D Exp. 01/20; 010118N Exp. 01/20

Recall Number: D-0795-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
16 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Envious, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955252023, NDC 57955-2523-2

Batch or Lot Expiration Information

Lot# Lot: 041217D Exp. 04/20

Recall Number: D-0893-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
7 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CS-Stomach, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955022022, NDC 57955-0220-2

Batch or Lot Expiration Information

Lot# Lot: 112916D Exp. 11/19

Recall Number: D-0803-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
73 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Mood Changes, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955202028, NDC 57955-2021-2

Batch or Lot Expiration Information

Lot# Lots: 051216N Exp. 05/19; 120816M Exp. 12/19

Recall Number: D-0558-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4507 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Back, Muscle & Joint Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955516125, NDC 57955-6161-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 012317H Exp. 01/20; 021418A Exp. 02/20; 033116F Exp. 03/19; 072216H Exp. 07/19; 102717C Exp. 10/19

Recall Number: D-0573-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1031 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Advanced First Aid, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955511823, NDC 57955-6000-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 021516A Exp. 02/19; 050216K Exp. 05/19; 081315Q exp. 08/18

Recall Number: D-0608-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
460 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Head Colds Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955528227, NDC 57955-5382-2

Batch or Lot Expiration Information

Lot# Lots: 030216B Exp. 03/19; 051018A Exp. 05/20; 091715D Exp. 09/18; 092815C Exp. 09/18

Recall Number: D-0944-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
38399 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #9 ER 911 Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4209-2

Batch or Lot Expiration Information

Lot# Lots: NR-031816A Exp. 03/19; NR-073015F Exp. 07/18; NR-010617H Exp. 01/20; NR-011216C Exp. 01/19; NR-021717F Exp. 02/20; NR-050916A Exp. 10/19; NR-061716A Exp. 06/19; NR-080116B Exp. 08/19; NR-090115L Exp. 09/18; NR-090616H Exp. 09/19; NR-101916B Exp. 10/19; NR-120815H Exp. 12/18

Recall Number: D-0529-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3281 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Bladder Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955504528, NDC 57955-1503-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 022616A Exp. 02/19; 030218D Exp. 03/20; 050216AC Exp. 05/19; 072216K Exp. 07/19; 083115H Exp. 08/18; 120717A Exp. 12/19; 123015C Exp. 12/18

Recall Number: D-0923-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1700 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #7 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-011916H Exp. 01/19; AUS-030816G Exp. 03/19; AUS-030917A Exp. 03/20; AUS-061016B Exp. 06/19; AUS-091515F Exp. 09/18; AUS-101116B Exp. 10/19

Recall Number: D-0951-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
14774 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #10 Scars-Adhesions Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4210-2

Batch or Lot Expiration Information

Lot# Lots: NR-031516E Exp. 03/19; NR-073015G Exp. 07/18; NR-010617J Exp. 01/20; NR-011216B Exp. 01/19; NR-040417F Exp. 04/20; NR-060517D Exp. 10/19; NR-061616H Exp. 06/19; NR-080116H Exp. 08/19; NR-090616J Exp. 09/19; NR-101416H Exp. 10/19; NR-120815G Exp. 12/18; NR-020118L Exp. 02/20; NR-022318H Exp. 02/20; NR-051618F Exp. 05/20; NR-081017N Exp. 08/19; NR-110117B Exp. 11/19

Recall Number: D-0920-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2600 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #4 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-011117D Exp. 01/20; AUS-011916D Exp. 01/19; AUS-030816D Exp. 03/19; AUS-050516D Exp. 05/19; AUS-061016A Exp. 06/19; AUS-081516E Exp. 08/19; AUS-091515D Exp. 09/18

Recall Number: D-0609-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
210 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Hair & Nails Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955504924, NDC 57955-5049-2

Batch or Lot Expiration Information

Lot# Lots: 030216C Exp. 03/19; 080916G Exp. 08/19

Recall Number: D-0745-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
268 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx ShinglePlex Skin, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955750123, NDC 57955-7501-2

Batch or Lot Expiration Information

Lot# Lots: 070815J Exp. 07/18; 091015G Exp. 09/18; 021216F Exp. 02/19; 052616M Exp. 05/19; 083016A Exp. 08/19

Recall Number: D-0934-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
700 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #3 (Blue Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-022418A Exp. 02/20; AUS-031618J Exp. 03/20; AUS-041718C Exp. 04/20; AUS-121417A Exp. 12/19

Recall Number: D-0736-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
138 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Migraine Freee..., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955002826, NDC 57955-0028-2

Batch or Lot Expiration Information

Lot# Lot: 020117H Exp. 02/20

Recall Number: D-0583-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
116 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Foul Bowel, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955531920, NDC 57955-5319-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 040616J Exp. 04/19; 080216D Exp. 08/19; 081015S Exp. 08/18

Recall Number: D-0816-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
197 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Calcium Metabolizer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955013129, NDC 57955-0131-2

Batch or Lot Expiration Information

Lot# Lots: 071316F Exp. 07/19; 120816B Exp. 12/19; 050216AD Exp. 05/19

Recall Number: D-0706-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4405 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Intense Anxiety Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955175025, NDC 57955-1751-2

Batch or Lot Expiration Information

Lot# Lots: 073015A Exp. 07/18; 123115F Exp. 12/18; 060916A Exp. 06/19; 042717A Exp. 04/20; 010118Y Exp. 01/20

Recall Number: D-0760-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
288 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies Great Lakes U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955260622, NDC 57955-2713-2

Batch or Lot Expiration Information

Lot# Lots: 060716F Exp. 06/19; 092216K Exp. 09/19; 022018D Exp. 02/20

Recall Number: D-0853-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
104 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Self-Abuse, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955107026, NDC 57955-1071-2

Batch or Lot Expiration Information

Lot# Lots: 072815P Exp. 07/18; 111016D Exp. 11/19

Recall Number: D-0906-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
895 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Safecare+ Southeast Regional Allergies Homeopathic Non-Drowsy Taste Free, Oral Spray, 1 fl oz (29.6 mL), UPC 357955834519, NDC 57955-8345-1

Batch or Lot Expiration Information

Lot# Lots: 013017K Exp. 01/20; 080515A Exp. 08/18

Recall Number: D-0626-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
101 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Athlete's Foot Fighter, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955512929, NDC 57955-5219-2

Batch or Lot Expiration Information

Lot# Lots: 020116B Exp. 02/19; 110116A Exp. 02/19; 123016B Exp. 12/19

Recall Number: D-0874-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
27 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Aller-Detox: Cosmetics & Household, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955240327, NDC 57955-2407-2

Batch or Lot Expiration Information

Lot# Lot: 081015L Exp. 08/18

Recall Number: D-0917-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1200 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #24 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-011916P Exp. 01/19; AUS-030816M Exp. 03/19; AUS-061016D Exp. 06/19; AUS-081516A Exp. 08/19

Recall Number: D-0822-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
20 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Complaining, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955230021, NDC 57955-2301-2

Batch or Lot Expiration Information

Lot# Lot: 052616/f Exp. 05/19

Recall Number: D-0635-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1393 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Total Body Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955536123, NDC 57955-5361-2

Batch or Lot Expiration Information

Lot# Lots: 052516L Exp. 05/19; 083115D Exp. 08/18; 091616Q Exp. 09/19; 110817A Exp. 11/19

Recall Number: D-0965-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2940 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Multi-Strain Flu Relief, 59 mL, (liquid/liquid), DIN-HM 80038065 UPC 357955180128

Batch or Lot Expiration Information

Lot# Lots: 011416H Exp. 01/19; 081516E Exp. 08/19

Recall Number: D-0628-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
936 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic CataClenz Eye Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955511229, NDC 57955-5112-2

Batch or Lot Expiration Information

Lot# Lots: 050216W Exp. 05/19; 080416B Exp. 08/19; 092216L Exp. 09/19; 101217A Exp. 10/19

Recall Number: D-0722-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
108 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Head Colds Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955028222, NDC 57955-0282-2

Batch or Lot Expiration Information

Lot# Lot: 011817B Exp. 01/20

Recall Number: D-0525-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4836 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Regional Allergies Rocky Mtns. U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955518624, NDC 57955-0200-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 0301817L Exp. 03/19; 030916G Exp. 03/19; 052615C Exp. 05/18; 080116B Exp. 08/19; 091015T Exp. 09/18

Recall Number: D-0532-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2045 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Heartburn Reliever, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955502227, NDC 57955-5022-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 020817H Exp. 02/20; 030816A Exp. 03/19; 050216B Exp. 05/19; 061616B Exp. 06/19; 072115C Exp. 07/18

Recall Number: D-0850-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
518 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Tinnitus Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955027522, NDC 57955-0275-2

Batch or Lot Expiration Information

Lot# Lots: 111417D Exp. 11/19; 070815D Exp. 07/18; 090816J Exp. 09/19

Recall Number: D-0643-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1005 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Constitutional Enhancer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955514923, NDC 57955-5149-2

Batch or Lot Expiration Information

Lot# Lots: 060316B Exp. 06/19; 072315B Exp. 07/18

Recall Number: D-0830-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
224 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies: Dairy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955219828, NDC 57955-2198-2

Batch or Lot Expiration Information

Lot# Lots: 073115B Exp. 07/18; 062116B Exp. 06/19; 121216C Exp. 12/19

Recall Number: D-0910-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
0

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Safecare+ Northeast Regional Allergies Non-Drowsy Homeopathic Taste-Free, Oral Spray, 1 fl oz (29.6 mL), UPC 357955832515, NDC 57955-8325-1

Batch or Lot Expiration Information

Lot# Lot: 070815H Exp. 07/18

Recall Number: D-0866-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
145 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CataCure, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955011224, NDC 57955-0112-2

Batch or Lot Expiration Information

Lot# Lots: 072815Y Exp. 07/18; 080916L Exp. 08/19

Recall Number: D-0926-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1200 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #1 (Yellow Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-041718A Exp. 04/20; AUS-071718N Exp. 07/20; AUS-111317C Exp. 11/19

Recall Number: D-0649-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
13 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Water Chemical Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955540021, NDC 57955-6100-2

Batch or Lot Expiration Information

Lot# Lots: 062816C Exp. 06/19

Recall Number: D-0734-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
143 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx TUBR Miasm, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955030423, NDC 57955-0304-2

Batch or Lot Expiration Information

Lot# Lots: 081815N Exp. 08/18; 080116D Exp. 08/19; 012517L Exp. 01/20

Recall Number: D-0683-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
18 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Tummy Aches Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955014621, NDC 57955-0146-2

Batch or Lot Expiration Information

Lot# Lots: 022316F Exp. 02/19

Recall Number: D-0867-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
201 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Mental Alertness For Seniors, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955156024, NDC 57955-1561-2

Batch or Lot Expiration Information

Lot# Lots: 072815R Exp. 07/18; 090116D Exp. 09/19

Recall Number: D-0676-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
45 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Bed Wetting Prevention Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955001225, NDC 57955-0012-2

Batch or Lot Expiration Information

Lot# Lots: 102216B Exp. 08/2018

Recall Number: D-0978-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
205 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Kids Aquaflora Candida Multi-Strain Formula, 118 mL (liquid), Manufactured by: King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, Imported by Ambiental Solutions, Inc. Vancouver, BC, V5Y 1E6, DIN-HM 80074869 UPC 357955181941

Batch or Lot Expiration Information

Lot# Lot: 040117A Exp. 04/20

Recall Number: D-0523-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
696 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Male Libido, 2 fl. oz. (59 mL), King Bio, Inc. 3 Westside Dr. Asheville, NC 28806, UPC 3579555101022, NDC 57955-5510-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 030216F Exp. 03/19; 051216K Exp. 05/19; 080315E Exp. 08/2018; 080916Q Exp. 08/2019; 120816E Exp. 12/19

Recall Number: D-0567-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
9068 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Acne Clear, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955504122, NDC 57955-5041-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 020116C Exp. 02/19; 033117C Exp. 03/20; 050216F Exp. 05/19; 072716D Exp. 07/19; 091416J Exp. 09/19; 101017D Exp. 10/19

Recall Number: D-0849-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
99 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies: Eggs & Meats, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955220220, NDC 57955-2207-2

Batch or Lot Expiration Information

Lot# Lots: 081715D Exp. 08/18; 071116E Exp. 07/19; 091616E Exp. 09/19

Recall Number: D-0666-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1141 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Kids Tummy Aches Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955514626, NDC 57955-4060-2

Batch or Lot Expiration Information

Lot# Lots: 021918B Exp. 02/2020; 050516D Exp. 05/2019; 072216Q Exp. 07/2019

Recall Number: D-0548-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
16184 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Sinus Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955513421, NDC 57955-5134-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 032217D Exp. 03/20; 033116B Exp. 03/19; 041518F Exp. 04/20; 061715D Exp. 06/18; 080116C Exp. 08/19; 100417A Exp. 10/19; 121916A Exp. 12/19

Recall Number: D-0641-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2368 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic TMJ/Jaw Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955503224, NDC 57955-5032-2

Batch or Lot Expiration Information

Lot# Lots: 060216C Exp. 06/19; 070815A Exp. 07/18; 123016E Exp. 12/19

Recall Number: D-0533-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1123 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Regional Allergies Plains U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955518585, NDC 57955-8199-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 030816B Exp. 03/19; 030817H Exp. 03/19; 092815A Exp. 09/18; 010118C Exp. 01/20

Recall Number: D-0637-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
14781 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Snore Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955512028, NDC 57955-5120-2

Batch or Lot Expiration Information

Lot# Lots: 052516Y Exp. 05/19; 060518C Exp. 06/20; 060917F Exp. 06/19; 070518A Exp. 07/20; 080317C Exp. 08/19; 081015B Exp. 08/18; 081815G Exp. 08/18; 111516C Exp. 11/19; 112317E Exp. 11/19

Recall Number: D-0855-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
38 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CS-Pain Reliever, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955021728, NDC 57955-0217-2

Batch or Lot Expiration Information

Lot# Lots: 071116H Exp. 07/19; 122216C Exp. 12/19

Recall Number: D-0825-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
145 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Hemorrhoid Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955002321, NDC 57955-0023-2

Batch or Lot Expiration Information

Lot# Lots: 052516P Exp. 05/19; 091316B Exp. 09/19

Recall Number: D-0975-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
77 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Hyperactive High Potency Homeopathic Formula, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955151029, NDC 57955-1511-2

Batch or Lot Expiration Information

Lot# Lots: 012317G Exp. 01/20

Recall Number: D-0790-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
50 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Easily Angered, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955102021, NDC 57955-1021-2

Batch or Lot Expiration Information

Lot# Lot: 041217C Exp. 04/20

Recall Number: D-0981-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4612 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Good Mood Enhancer Homeopathic, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955515029, NDC 57955-8150-2

Batch or Lot Expiration Information

Lot# Lots: 041117E Exp. 04/20; 030118H Exp. 03/20; 040616F Exp. 04/19; 071316N Exp. 07/19; 111617C Exp. 11/19

Recall Number: D-0768-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
795 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx ParaClenz, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955001621, NDC 57955-0193-2

Batch or Lot Expiration Information

Lot# Lots: 081015J Exp. 08/18; 062816A Exp. 06/19; 101716B Exp. 10/19; 030718A Exp. 03/20

Recall Number: D-0840-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Prejudiced, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955100027, NDC 57955-2322-2

Batch or Lot Expiration Information

Lot# Lot: 062615D Exp. Unknown

Recall Number: D-0695-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2853 tubes

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Eczema Symptom Relief Homeopathic Topical Lotion, 3 oz. (85 g), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955092131, NDC 57955-0921-3

Batch or Lot Expiration Information

Lot# Lots: 010918ZZ Exp. 01/20; 021317ZZ Exp. 02/19; 090717ZZ Exp. 09/19

Recall Number: D-0961-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3020 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Arthritis Pain & Joint Relief Soulagement De La Douleur Arthritique et Articulaire, 59 mL, (liquid/liquid) DIN-HM 80035118 UPC 357955180425

Batch or Lot Expiration Information

Lot# Lots: 011516A Exp. 01/19; 081516F Exp. 08/19

Recall Number: D-0665-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
32 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine for kids! Chicken Pox Symptom Relief Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955602521, NDC 57955-6025-2

Batch or Lot Expiration Information

Lot# Lots: 021216K Exp. 02/2019; 062716D Exp. 06/2019

Recall Number: D-0755-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
244 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Bone Strengthener, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955007029, NDC 57955-0070-2

Batch or Lot Expiration Information

Lot# Lots: 060316F Exp. 06/19; 022316B Exp. 02/19; 122216H Exp. 12/19

Recall Number: D-0563-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
198 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Eye Stress, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955515128, NDC 57955-5151-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 033116P Exp. 03/19; 110916B Exp. 11/19

Recall Number: D-0774-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
57 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CS-Skin, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955021926, NDC 57955-0224-2

Batch or Lot Expiration Information

Lot# Lots: 120715B Exp. 12/18; 022616B Exp. 02/19

Recall Number: D-0957-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
5106 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #24 Day & Night Vitals Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4214-2

Batch or Lot Expiration Information

Lot# Lots: NR-020118R Exp. 02/20; NR-071318A Exp. 07/20; NR-071318C Exp. 07/20; NR-092517A Exp. 09/19; NR-110117E Exp. 11/19; NR-120317P Exp. 12/19

Recall Number: D-0885-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
262 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Smoke Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955303022, NDC 57955-3031-2

Batch or Lot Expiration Information

Lot# Lots: 091015N Exp. 09/18; 111716H Exp. 11/19

Recall Number: D-0839-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
17 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx FertiCare, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000525, NDC 57955-0005-2

Batch or Lot Expiration Information

Lot# Lot: 062615E Exp. 06/18

Recall Number: D-0739-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
95 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx LymePlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006923, NDC 57955-0069-2

Batch or Lot Expiration Information

Lot# Lots: 072815F Exp. 07/18; 061716C Exp. 06/19; 020817D Exp. 02/20; 030518F Exp. 03/20

Recall Number: D-0544-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1339 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Scar Freee, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955508724, NDC 57955-5087-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 031516B Exp. 03/19; 041817A Exp. 04/20; 050216H Exp. 05/19; 081117B Exp. 08/19; 091015D Exp. 09/18

Recall Number: D-0782-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
557 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Urinary Tract Infections, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955005223, NDC 57955-0052-2

Batch or Lot Expiration Information

Lot# Lots: 072815J Exp. 07/18; 030916Y Exp. 03/19; 110716B Exp. 11/19; 101317J Exp. 10/19

Recall Number: D-0655-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
453 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Allergy & Red Eye Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955516422, NDC 57955-5164-2

Batch or Lot Expiration Information

Lot# Lots: 081117A Exp. 08/19; 123016A Exp. 12/19

Recall Number: D-0688-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
15 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Chicken Pox Symptom Relief Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955782520, NDC 57955-7825-2

Batch or Lot Expiration Information

Lot# Lots: 042616D Exp. 04/19

Recall Number: D-0653-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
14 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Female Discomforts, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955500728, NDC 57955-5007-2

Batch or Lot Expiration Information

Lot# Lots: 080116A Exp. 08/19

Recall Number: D-0710-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
126 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Stye Freee..., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955012528, NDC 57955-0132-2

Batch or Lot Expiration Information

Lot# Lots: 083115B Exp. 08/18; 061716A Exp. 06/19; 120516B Exp. 12/19; 010418F Exp. 01/20

Recall Number: D-0648-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
35 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Climate Adaptation Hot & Dry, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955528623, NDC 57955-0172-2

Batch or Lot Expiration Information

Lot# Lots: 062415V Exp. 06/18

Recall Number: D-0781-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
693 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Good Mood Enhancer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955208020, NDC 57955-2080-2

Batch or Lot Expiration Information

Lot# Lots: 050317A Exp. 05/20; 072815S Exp. 07/18; 031016F Exp. 03/19; 071116G Exp. 07/19

Recall Number: D-0757-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
936 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Total Body Detox Cleansing & Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955036128, NDC 57955-0361-2

Batch or Lot Expiration Information

Lot# Lots: 022117K Exp. 02/20; 120316F Exp. 12/19; 040117B

Recall Number: D-0933-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
190 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #25 (Yellow, White and Purple Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A. Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lot: AUS-122017A Exp. 12/19

Recall Number: D-0601-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
718 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Paralixer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955501626, NDC 57955-5016-2

Batch or Lot Expiration Information

Lot# Lots: 010118Z Exp. 01/20; 012616D Exp. 01/2019; 021717B Exp. 0919; 091216E Exp. 09/2019

Recall Number: D-0619-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2533 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Cough Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955516620, NDC 57955-5166-2

Batch or Lot Expiration Information

Lot# Lots: 012516A Exp. 01/19; 090816D Exp. 09/19

Recall Number: D-0551-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
556 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic EMF Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955597520, NDC 57955-5975-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 032816E Exp. 03/19; 033116M Exp. 03/19; 062817A Exp. 06/19

Recall Number: D-0737-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1244 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Sleep Aid, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955263920, NDC 57955-2640-2

Batch or Lot Expiration Information

Lot# Lots: 022318F Exp. 02/20; 020416A Exp. 02/19; 080916N Exp. 08/19

Recall Number: D-0694-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1732 tubes

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Psoriasis Symptom Relief Homeopathic Topical Lotion, 3 oz. (85 g), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955092032, NDC 57955-0920-3

Batch or Lot Expiration Information

Lot# Lots: 013018ZZ Exp. 01/20; 021217ZZ Exp. 02/19; 110717ZZ Exp. 11/19

Recall Number: D-0671-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3071 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Kids Stress & Anxiety Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955042327, NDC 57955-0423-2

Batch or Lot Expiration Information

Lot# Lots: 070516E Exp. 07/2019; 081016G Exp. 08/2019

Recall Number: D-0726-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
388 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Wounds Recovery, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955011828, NDC 57955-0118-2

Batch or Lot Expiration Information

Lot# Lots: 081815M Exp. 08/18; 012017B Exp. 01/20

Recall Number: D-0809-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
970 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Cough Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955016625, NDC 57955-0166-2

Batch or Lot Expiration Information

Lot# Lots: 102116A Exp. 10/19; 063015D Exp. 06/18; 123115E Exp. 12/18; 051716L Exp. 05/19; 022117L Exp. 02/20

Recall Number: D-0661-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
893 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Children's Appetite Enhancer for kids! Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955531821, NDC 57955-5318-2

Batch or Lot Expiration Information

Lot# Lots: 020117F Exp. 02/2020; 060216E Exp. 06/2019; 080916B Exp. 08/2019; 092415F Exp. 09/2018

Recall Number: D-0733-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
29 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Repressed Sexual Issues Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955126027, NDC 57955-1261-2

Batch or Lot Expiration Information

Lot# Lots: 061716B Exp. 06/19; 012517K Exp. 01/20

Recall Number: D-0743-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
98 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Breast Cyst & Discomforts, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000327, NDC 57955-0003-2

Batch or Lot Expiration Information

Lot# Lots: 091515A Exp. 09/18; 010517B Exp. 01/20

Recall Number: D-0780-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Gossipy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955225027, NDC 57955-2251-2

Batch or Lot Expiration Information

Lot# Lot: 031016F Exp. 03/19

Recall Number: D-0971-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
422 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies Pacific U.S. Homeopathic, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955260820, NDC 57955-2717-2

Batch or Lot Expiration Information

Lot# Lots: 030518R Exp. 03/20; 062415F Exp. 06/18; 072015B Exp. 07/18

Recall Number: D-0720-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1018 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Back, Neck, Muscle & Joint Injuries, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955016120, NDC 57955-0261-2

Batch or Lot Expiration Information

Lot# Lots: 011518C Exp. 01/20; 081815J Exp. 08/18; 032216F Exp. 03/19; 091616P Exp. 09/19

Recall Number: D-0566-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
35 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Eggs & Meats Intolerances, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955522027, NDC 57955-0723-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 033116S Exp. 03/19; 063016M Exp. 06/19

Recall Number: D-0754-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
794 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Constitutional Enhancer Constitution, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955014928, NDC 57955-0149-2

Batch or Lot Expiration Information

Lot# Lots: 102016F Exp. 10/19; 022316D Exp. 02/19; 061716D Exp. 06/19

Recall Number: D-0576-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1249 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Artery, Cholesterol & BP, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955506423, NDC 57955-5064-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 050216C Exp. 07/19; 071316K Exp. 05/19

Recall Number: D-0878-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
130 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Appetite Enhancer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955012825, NDC 57955-0128-2

Batch or Lot Expiration Information

Lot# Lots: 091015C Exp. 09/18; 082516B Exp. 08/19; 022317F Exp. 02/20

Recall Number: D-0574-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
291 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Muscle Maximizer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955513322, NDC 57955-5133-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 010118AE Exp. 01/20; 050216L Exp. 05/2019; 092216E Exp. 09/2019

Recall Number: D-0670-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
124 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine for kids! Children's Growth & Development Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955514220, NDC 57955-5142-2

Batch or Lot Expiration Information

Lot# Lots: 072516E Exp. 07/2019; 050516E Exp. 05/2019

Recall Number: D-0526-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
6584 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Cold Sores & Herpes, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955516521, NDC 57955-5165-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 030218B Exp. 03/20; 033116H Exp. 03/19; 061815J Exp. 06/18; 062716B Exp. 06/19; 091616C Exp. 09/19; 111017B Exp. 11/19; 123015A Exp. 12/18

Recall Number: D-0887-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
53 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Physical Anger, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955101024, NDC 57955-1011-2

Batch or Lot Expiration Information

Lot# Lots: 112117A Exp. 11/19; 091015E Exp. 09/18

Recall Number: D-0824-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
193 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Bio Reset/Jet Lag, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955012627, NDC 57955-0126-2

Batch or Lot Expiration Information

Lot# Lots: 022316C Exp. 02/19; 052516Q Exp. 05/19; 102016E Exp. 10/19; 112117G Exp. 11/19

Recall Number: D-0678-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
659 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Lower GI Restoration Digestion High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955032021, NDC 57955-0322-2

Batch or Lot Expiration Information

Lot# Lots: 030916J Exp. 03/19; 072516D Exp. 07/19; 121717A Exp. 12/19

Recall Number: D-0924-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3800 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #8 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-011117F Exp. 01/20; AUS-011916G Exp. 01/19; AUS-030816H Exp. 03/19; AUS-030917B Exp. 03/20; AUS-050516G Exp. 05/19; AUS-082616A Exp. 08/19; AUS-091515G Exp. 09/18

Recall Number: D-0791-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
345 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Constipation Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955001928, NDC 57955-0019-2

Batch or Lot Expiration Information

Lot# Lots: 072815L Exp. 07/18; 041416L Exp. 04/19; 082916B Exp. 08/19

Recall Number: D-0697-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3536 tubes

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Soothing Advanced Arnica Pure Homeopathic Cream High Potency Homeopathic Formula for Professional Use Only, 3 oz. (85 g), King Bio, Inc., 3 Westside Drive Asheville, NC 28806 USA, UPC 357955730132, NDC 57955-7301-3

Batch or Lot Expiration Information

Lot# Lots: 010517ZZ Exp. 01/20; 030818ZZ Exp. 03/21; 040617ZZ Exp. 04/20; 100616ZZ Exp. 05/19; 110916ZZ Exp. 11/19

Recall Number: D-0773-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
37 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CS-Brain, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955021223, NDC 57955-0222-2

Batch or Lot Expiration Information

Lot# Lots: 022616C Exp. 02/19; 122216E Exp. 12/19

Recall Number: D-0689-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
95 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Children's Fever Reliever Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955015925, NDC 57955-0176-2

Batch or Lot Expiration Information

Lot# Lots: 082516A Exp. 08/2019; 102015F Exp. 10/2018

Recall Number: D-0778-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
30 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Hypochondria, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955180029, NDC 57955-1807-2

Batch or Lot Expiration Information

Lot# Lots: 031016H Exp. 03/19; 103116A Exp. 10/19

Recall Number: D-0956-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
12548 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #8 Allergy (Blue Label) Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4208-2

Batch or Lot Expiration Information

Lot# Lots: NR-020618A Exp. 02/20; NR-051618E Exp. 05/20; NR-051818B Exp. 05/20; NR-101117D Exp. 10/19; NR-020118J Exp. 02/20; NR-092717B Exp. 09/19

Recall Number: D-0793-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
245 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Heartburn Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955002222, NDC 57955-0022-2

Batch or Lot Expiration Information

Lot# Lots: 041416B Exp. 04/19; 091416K Exp. 09/19

Recall Number: D-0969-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
770 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Regional Allergies Western Canada, 59 mL, (liquid/liquide), DIN-HM 80074875 UPC 357955181828

Batch or Lot Expiration Information

Lot# Lot: 021517M Exp. 02/20

Recall Number: D-0679-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1937 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Influenza Multi-Strain Flu Medicine Immune High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955019923, NDC 57955-0298-2

Batch or Lot Expiration Information

Lot# Lots: 011618A Exp. 01/20; 111617H Exp. 11/19; 122216A Exp. 12/19

Recall Number: D-0702-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2027 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies Southern U.S. Allergy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955260127, NDC 57955-2721-2

Batch or Lot Expiration Information

Lot# Lots: 050216AA Exp. 05/19; 101116B Exp. 10/19; 010118K Exp. 01/20

Recall Number: D-0629-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4888 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Adrenal Burnout, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955597926, NDC 57955-1434-2

Batch or Lot Expiration Information

Lot# Lots: 050218E Exp. 05/20; 080317E Exp. 08/19; 120216A Exp. 12/19; 120217F Exp. 12/19

Recall Number: D-0541-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2870 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Liver Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955006220, NDC 57955-5062-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 012616H Exp. 01/19; 031017C Exp. 03/20; 052516AB Exp. 05/19; 083115G Exp. 08/18; 083116D Exp. 08/19; 010118R Exp. 01/20

Recall Number: D-0811-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
842 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies Northest U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955260721, NDC 57955-2707-2

Batch or Lot Expiration Information

Lot# Lots: 051716G Exp. 05/19; 072516H Exp. 07/19; 081117C Exp. 08/19

Recall Number: D-0547-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
41 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Shellfish & Seafood Intolerances, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955520122, NDC 57955-0726-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 032216A Exp. 03/19; 063016L Exp. 06/19

Recall Number: D-0783-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
96 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Aller-Detox: Food Addititives & Preservatives, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955240525, NDC 57955-2405-2

Batch or Lot Expiration Information

Lot# Lots: 030916N Exp. 03/19; 121217A Exp. 12/19

Recall Number: D-0896-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
20 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Claustrophobia, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955182023, NDC 57955-1822-2

Batch or Lot Expiration Information

Lot# Lot: 120816D Exp. 12/19

Recall Number: D-0610-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
400 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Grief & Guilt Reliever, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955503828, NDC 57955-5038-2

Batch or Lot Expiration Information

Lot# Lots: 022417G Exp. 02/20; 052516N Exp. 05/19; 080416D Exp. 08/19

Recall Number: D-0845-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
91 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Stubborn & Contentious, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955103028, NDC 57955-1031-2

Batch or Lot Expiration Information

Lot# Lots: 062316A Exp. 06/19; 101716D Exp. 10/19; 122216D Exp. 12/19

Recall Number: D-0656-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
283 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Odor Freee, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955513025, NDC 57955-5130-2

Batch or Lot Expiration Information

Lot# Lots: 102816H Exp. 10/2019; 123016D Exp. 12/2019

Recall Number: D-0611-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
5190 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Gout Symptom Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955502128, NDC 57955-6021-2

Batch or Lot Expiration Information

Lot# Lots: 020118D Exp. 02/20; 071415A Exp. 07/18; 080317C Exp. 08/2019

Recall Number: D-0620-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
73 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Cosmetic & Household Detox, 2 fl. oz. (59 mL), King Bio, Inc. 3 Westside Dr. Asheville, NC 28806, UPC 357955540328, NDC 57955-6103-2

Batch or Lot Expiration Information

Lot# Lots: 021816B Exp. 02/19; 051216Q Exp. 05/19

Recall Number: D-0568-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
478 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Mental Alertness for Seniors, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955595625, NDC 57955-5956-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 021016K Exp. 02/19; 022317G Exp. 02/2020; 040115C Exp. 04/2018; 062416B Exp. 06/19; 112315D Exp. 11/2018

Recall Number: D-0581-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
11321 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Allergy & Hay Fever Reliever, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955504320, NDC 57955-5043-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 051016D Exp. 05/19; 052517D Exp. 05/20; 071316J Exp. 07/19; 082015D Exp. 0818; 041618A Exp. 04/20; 101017F Exp. 10/19

Recall Number: D-0521-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
105716 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's aquaflora Candida High Potency, 8 fl. oz. (236 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 35795580018, NDC 57955-8020-89

Batch or Lot Expiration Information

Lot# Lot Numbers: 120217R Exp. 12/19; 102017C Exp. 10/19; 101017G Exp. 10/19; 111417C Exp. 11/19; 062818E Exp. 06/20; 122817B Exp. 12/19; 030818B Exp. 03/20; 010716A Exp. 01/19; 011617H Exp. 01/20; 012517M Exp. 01/20; 020717A Exp. 02/20; 021816A Exp. 02/19; 031016C Exp. 03/19; 031016D Exp. 03/19; 033016K Exp. 03/19; 052516J Exp. 05/19; 052918G Exp. 05/20; 062116A Exp. 06/19; 062818A Exp. 06/20; 062818F Exp. 06/20; 090816B Exp. 06/20; 101216A Exp. 10/19; 112315A Exp. 11/18; 112916C Exp. 11/19; 120816N Exp. 12/19

Recall Number: D-0729-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
23 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Paranoid Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955226024, NDC 57955-2261-2

Batch or Lot Expiration Information

Lot# Lots: 040616B Exp. 04/19; 012317D Exp. 01/20

Recall Number: D-0746-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
198 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Snore Control Sleep, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955012023, NDC 57955-0120-2

Batch or Lot Expiration Information

Lot# Lots: 021616B Exp. 02/19; 083016B Exp. 08/19

Recall Number: D-0553-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4119 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Menopause Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955500629, NDC 57955-6006-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 033016J Exp. 03/19; 052516T Exp. 05/19; 080916D Exp. 08/2019; 090915B Exp. 09/18; 110117F Exp. 11/19

Recall Number: D-0819-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
45 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Morning Sickness, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000822, NDC 57955-0008-2

Batch or Lot Expiration Information

Lot# Lot: 061616F Exp. 06/19

Recall Number: D-0938-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
503 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #7 (Aqua Blue Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-020118D Exp. 02/20; AUS-110817A Exp. 11/19

Recall Number: D-0806-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
561 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Advanced Arnica, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955730323, NDC 57955-7304-2

Batch or Lot Expiration Information

Lot# Lots: 040118A Exp. 04/20; 060616C Exp. 06/19; 110117F Exp. 11/19

Recall Number: D-0687-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
45 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Children's Ear Relief Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955075721, NDC 57955-0758-2

Batch or Lot Expiration Information

Lot# Lots: 032316B Exp. 03/19

Recall Number: D-0913-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1700 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #11 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-050516J Exp. 05/19; AUS-030917D Exp. 03/20; AUS-011916L Exp. 01/19; AUS-011117H Exp. 01/20

Recall Number: D-0613-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
243 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Food Intolerances, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955072720, NDC 57955-0727-2

Batch or Lot Expiration Information

Lot# Lots: 011216A Exp. 01/19; 030117Q Exp. 03/20; 050216T Exp. 05/19; 060716H Exp. 06/19; 093016A Exp. 09/19

Recall Number: D-0848-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
338 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Nausea & Motion Sickness, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955005520, NDC 57955-0055-2

Batch or Lot Expiration Information

Lot# Lots: 072815T Exp. 07/18; 071116F Exp. 07/19; 122216F Exp. 12/19

Recall Number: D-0598-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
18449 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Sleep Aid, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955503927, NDC 57955-5839-2

Batch or Lot Expiration Information

Lot# Lots: 021016E Exp. 02/19; 060118C Exp. 06/20; 060518A Exp. 06/20; 071318G Exp. 07/20; 080717A Exp. 08/19; 081315N Exp. 08/18; 111516J Exp. 11/19; 122017A Exp. 12/2019; 122915D Exp. 12/18

Recall Number: D-0693-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3211 tubes

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Rosacea Symptom Relief Homeopathic Topical Lotion, 3 oz. (85 g), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955091936, NDC 57955-0919-3

Batch or Lot Expiration Information

Lot# Lots: 021117ZZ Exp. 02/19; 031918ZZ Exp. 03/20; 110217ZZ Exp. 09/19

Recall Number: D-0642-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
377 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Jet Lag & Shift Change, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955512622, NDC 57955-5126-2

Batch or Lot Expiration Information

Lot# Lots: 060216D Exp. 06/19

Recall Number: D-0835-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Calloused, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955231028, NDC 57955-2311-2

Batch or Lot Expiration Information

Lot# Lot: 063016C Exp. 06/19

Recall Number: D-0868-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
10 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Environmental Adaptation Cold/Dry, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955028321, NDC 57955-0288-2

Batch or Lot Expiration Information

Lot# Lot: 062916E Exp. 06/19

Recall Number: D-0716-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
456 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Blood & Kidney Detox Cleansing & Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006121, NDC 57955-0190-2

Batch or Lot Expiration Information

Lot# Lots: 071116A Exp. 07/19; 010818B Exp. 01/20

Recall Number: D-0549-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
425 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Ear Relief Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955515722, NDC 57955-0918-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 032816B Exp. 03/19; 101917B Exp. 10/19

Recall Number: D-0538-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2177 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Skin Irritations & Itch Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955516828, NDC 57955-5168-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 010818C Exp. 01/20; 030916S Exp. 08/18; 041117K Exp. 04/19; 072216M Exp. 07/19; 083115F Exp. 08/18

Recall Number: D-0976-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
199 tubes

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Advanced Arnica Super Arnica, 59 mL, Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 Imported by Ambiental Solutions, Inc. Vancouver, BC, V5Y 1E6, DIN-HM 800774304 UPC 357955181330

Batch or Lot Expiration Information

Lot# Lot: 050117ZZ Exp. 05/20

Recall Number: D-0669-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
144 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine for kids! Nosebleed Relief Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955514022, NDC 57955-5140-2

Batch or Lot Expiration Information

Lot# Lots: 050516H Exp. 05/2019; 080916J Exp. 08/2019

Recall Number: D-0980-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
349 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Bug Away Homeopathic, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955507726, NDC 57955-5077-2

Batch or Lot Expiration Information

Lot# Lots: 071116B Exp. 07/19; 050516B Exp. 05/19; 020116A Exp. 07/19

Recall Number: D-0817-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
269 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies: Grains & Gluten, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955220329, NDC 57955-2203-2

Batch or Lot Expiration Information

Lot# Lots: 112916B Exp. 11/19; 041416E Exp. 04/19

Recall Number: D-0950-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
11489 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #6 Para Solve Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4206-2

Batch or Lot Expiration Information

Lot# Lots: NR-031516H Exp. 03/19; NR-011216G Exp. 01/19; NR-021717C Exp. 02/20; NR-040417D Exp. 04/20; NR-061616E Exp. 06/19; NR-090115H Exp. 09/19; NR-090616E Exp. 09/19; NR-101416F Exp. 10/19; NR-120815L Exp. 12/18; NR-020118F Exp. 02/20; NR-022318F Exp. 02/20; NR-052218A Exp. 05/20; NR-071718G Exp. 07/20; NR-101117G Exp. 10/19; NR-120317F Exp. 02/19; NR-110117D Exp. 11/19

Recall Number: D-0912-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1400 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #10 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-101316A Exp. 10/19; AUS-062317B Exp. 06/20; AUS-061016C Exp. 06/19; AUS-030816K Exp. 03/19; AUS-011916K Exp. 01/19

Recall Number: D-0818-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
20 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Immature, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955229025, NDC 57955-2291-2

Batch or Lot Expiration Information

Lot# Lot: 060716J Exp. 06/19

Recall Number: D-0796-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
12 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Extravagant, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955233022, NDC 57955-2331-2

Batch or Lot Expiration Information

Lot# Lot: 040616O Exp. 04/19

Recall Number: D-0578-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
490 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Bone Strengthener, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955507029, NDC 57955-5070-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 030118N Exp. 03/20; 042616A Exp. 04/19; 070516B Exp. 07/19; 070815B Exp. 07/18; 101317H Exp. 10/19

Recall Number: D-0901-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2248 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Aquaflora Phase II Candida Control Program, Net 16 fl. oz. (1 PT) 473 mL, Homeopathic Formula, Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955160267, NDC 57955-1602-6

Batch or Lot Expiration Information

Lot# Lots: 010518G Exp. 07/18; 011617F Exp. 01/20; 021016G Exp. 02/19; 051716P Exp. 02/19; 072315A Exp. 07/18

Recall Number: D-0982-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
9405 bags

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Leg Cramp & Spasm Relief Homeopathic, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955543527, NDC 57955-6035-2

Batch or Lot Expiration Information

Lot# Lots: 102816D Exp. 10/19; 050516F Exp. 05/19; 101416A Exp. 10/19; 123115D Exp. 12/18; 041518J Exp. 04/20

Recall Number: D-0919-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2900 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #3 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-011117C Exp. 01/20; AUS-011916C Exp. 01/19; AUS-030816C Exp. 03/19; AUS-050516C Exp. 05/19; AUS-061217A Exp. 06/20; AUS-081516F Exp. 08/19; AUS-091515C Exp. 09/18

Recall Number: D-0554-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
26410 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Appetite & Weight with P.H.A.T., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955515623, NDC 57955-5181-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 021718D Exp. 02/20; 112317C Exp. 11/19; 012616G Exp. 01/19; 033116A Exp. 03/19; 052517F Exp. 05/20; 072916D Exp. 07/19; 091415H Exp. 09/18; 091616A Exp. 09/19; 121916C Exp. 12/19

Recall Number: D-0915-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2500 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #2 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-011916B Exp. 01/19; AUS-011117B Exp. 01/20; AUS-030816B Exp. 03/19; AUS-050516B Exp. 05/19; AUS-081516G Exp. 08/19; AUS-091515B Exp. 09/18

Recall Number: D-0959-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
192 tubes

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Acute Pain Relief Cooling Topical, 89 mL (topical cream), Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 Imported by Ambiental Solutions, Inc. Vancouver, BC, V5Y 1E6, DIN-HM 80074489 UPC 357955181439

Batch or Lot Expiration Information

Lot# Lot: 020417ZZ Exp. 02/20

Recall Number: D-0799-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
112 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies Desert U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955260424, NDC 57955-2704-2

Batch or Lot Expiration Information

Lot# Lots: 040118C Exp. 04/20; 031417B Exp. 03/20

Recall Number: D-0797-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
6 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
SafeCareRx Nostalgia, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955278023, NDC 57955-2781-2

Batch or Lot Expiration Information

Lot# Lot: 040616M Exp. 04/19

Recall Number: D-0918-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
600 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #25 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-011916Q Exp. 01/19; AUS-061016E Exp. 06/19

Recall Number: D-0929-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
997 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #12 (Pink Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-072018G Exp. 07/20; AUS-100117E Exp. 10/19

Recall Number: D-0622-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
39 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Climate Adaptation Cold & Dry, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955528326, NDC 57955-5283-2

Batch or Lot Expiration Information

Lot# Lots: 021216L Exp. 02/19; 062415Z Exp. 06/18

Recall Number: D-0751-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
351 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Male Strengthener, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955001027, NDC 57955-0010-2

Batch or Lot Expiration Information

Lot# Lots: 080916F Exp. 08/19; 062215C Exp. 06/18; 021616F Exp. 02/19

Recall Number: D-0888-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
142 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Sporting Edge, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 35795500312, NDC 57955-0031-2

Batch or Lot Expiration Information

Lot# Lots: 122815C Exp. 12/18; 101716A Exp. 10/19

Recall Number: D-0921-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2200 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #5 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-011117E Exp. 01/20; AUS-011916E Exp. 01/19; AUS-030816E Exp. 03/19; AUS-050516E Exp. 05/19; AUS-101116A Exp. 10/19

Recall Number: D-0769-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
35 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Nosebleed Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955014027, NDC 57955-0140-2

Batch or Lot Expiration Information

Lot# Lots: 051716K Exp. 05/19; 030317A Exp. 03/20

Recall Number: D-0851-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Gambling, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955301028, NDC 57955-3011-2

Batch or Lot Expiration Information

Lot# Lot: 063016G Exp. 06/19

Recall Number: D-0606-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
213 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Mental Alertness, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955505426, NDC 57955-5954-2

Batch or Lot Expiration Information

Lot# Lots: 021016H Exp.02/19; 061316A Exp. 06/2019

Recall Number: D-0527-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
550 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Menstrual Cramps & Irregularities 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955500421, NDC 57955-5004-02

Batch or Lot Expiration Information

Lot# Lot Numbers: 041416J Exp. 04/19; 070816F Exp. 07/19; 091015K Exp. 09/2018; 030218C Exp. 03/20

Recall Number: D-0582-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
9405 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Leg Cramp & Spasm Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955543527, NDC 57955-6035-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 041518J Exp. 04/20; 050516F Exp. 05/19; 101416A Exp. 10/19; 102816D Exp. 10/19; 123115D Exp. 12/18

Recall Number: D-0546-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
45 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Nuts & Seeds Intolerances, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955520528, NDC 57955-5205-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 022117E Exp. 02/2020; 032216B Exp. 03/19; 072716E Exp. 07/2019

Recall Number: D-0708-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
790 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Skin Irritations & Itch Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955175025, NDC 57955-0177-2

Batch or Lot Expiration Information

Lot# Lots: 080916V Exp. 08/19; 010418C Exp. 01/20; 022616G Exp. 02/19

Recall Number: D-0663-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
873 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine for kids! Children's Fever Reliever Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955515920, NDC 57955-5159-2

Batch or Lot Expiration Information

Lot# Lots: 021216H Exp. 02/2019; 052616H Exp. 05/2019; 102815C Exp. 10/2018; 120816A Exp. 12/2019

Recall Number: D-0789-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
17 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Eating Disorders, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000129, NDC 57955-0001-2

Batch or Lot Expiration Information

Lot# Lot: 040606L Exp. 04/19

Recall Number: D-0823-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
144 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Menstrual Cramps & Irregularities, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000426, NDC 57955-0004-2

Batch or Lot Expiration Information

Lot# Lots: 083116E Exp. 08/19; 052616D Exp. 05/19

Recall Number: D-0869-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
115 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Environmental Adaptation Hot/Humid, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955028529, NDC 57955-0285-2

Batch or Lot Expiration Information

Lot# Lots; 081015K Exp. 08/18; 071316H Exp. 07/19; 111716J Exp. 11/19

Recall Number: D-0630-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
248 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic ChemoClenz, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955507123, NDC 57955-5071-2

Batch or Lot Expiration Information

Lot# Lots: 050516A Exp. 05/19

Recall Number: D-0939-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1500 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #8 (Royal Blue Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A. Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-031618B Exp. 03/20; AUS-020118E Exp. 02/20; AUS-041718G Exp. 04/20; AUS-071718W Exp. 07/20; AUS-100117B Exp. 10/19

Recall Number: D-0586-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
834 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Water Retention, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955507826, NDC 57955-5078-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 012616K Exp. 01/19; 040616H Exp. 04/19; 073015B Exp. 07/18

Recall Number: D-0844-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
492 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Teeth & Gum Formula, 2 fl. oz. (59 mL), NDC 57955-0073-2 UPC 357955007326 King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA

Batch or Lot Expiration Information

Lot# Lots: 062415E Exp. 06/18; 071116D Exp. 07/18; 121317H Exp. 12/19

Recall Number: D-0954-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
21870 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #4 Wood Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4204-2

Batch or Lot Expiration Information

Lot# Lots: NR-031516K Exp. 03/19; NR-010617D Exp. 01/20; NR-011216J Exp. 01/19; NR-021717B Exp. 02/20; NR-051116A Exp. 05/19; NR-060217C Exp. 06/20; NR-061616C Exp. 06/19; NR-080116G Exp. 08/19; NR-090215A Exp. 09/18; NR-090616D Exp. 09/19; NR-101416D Exp. 10/19; NR-120815P Exp. 12/18; NR-081017D Exp. 08/19; NR-020118D Exp. 02/20; NR-071018A Exp. 07/20; NR-071018C Exp. 07/20; NR-071018E Exp. 07/20; NR-110317A Exp. 11/19; NR-120317D Exp. 12/19

Recall Number: D-0940-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2000 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #9 (Fuschia Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-020118F Exp. 02/20; AUS-071718Y Exp. 07/20; AUS-100117C Exp. 10/19

Recall Number: D-0930-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
800 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #2 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lot: AUS-111517D Exp. 11/19

Recall Number: D-0559-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
8221 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Arthritis Pain & Joint Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955516224, NDC 57955-6162-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 022417L Exp. 02/20; 033116G Exp. 03/19; 062316C 06/19; 080917D Exp. 08/19; 091616B Exp. 09/19; 112117L Exp. 11/19

Recall Number: D-0603-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1663 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Nausea & Motion Sickness, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955505525, NDC 57955-5055-2

Batch or Lot Expiration Information

Lot# Lots: 020916P Exp. 02/19; 072216P Exp. 07/19; 010518P Exp. 01/20

Recall Number: D-0698-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
756 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Upper GI Restoration Digestion High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive Asheville, NC 28806 USA, UPC 357955032120, NDC 57955-0325-2

Batch or Lot Expiration Information

Lot# Lots: 051716U Exp. 05/19; 073115C Exp. 07/18; 080216C Exp. 08/19; 120217N Exp. 12/19

Recall Number: D-0651-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
15 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Climate Adaptation Cold & Damp, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955528425, NDC 57955-0170-2

Batch or Lot Expiration Information

Lot# Lots: 071316G Exp. 07/19

Recall Number: D-0714-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
338 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Anti-Aging & Wrinkles For Women, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955614722, NDC 57955-6148-2

Batch or Lot Expiration Information

Lot# Lots: 032316A Exp. 03/19; 010617B Exp. 01/20

Recall Number: D-0704-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
463 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Sugar Metabolizer Men/Women, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955007227, NDC 57955-0365-2

Batch or Lot Expiration Information

Lot# Lots: 091015J Exp. 09/18; 060216A Exp. 06/19; 091216H Exp. 09/19; 010118X Exp. 01/20

Recall Number: D-0828-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
114 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Female Enhancer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955011521, NDC 57955-0115-2

Batch or Lot Expiration Information

Lot# Lots: 060316A Exp. 06/19; 120116A Exp. 12/19

Recall Number: D-0740-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
12 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Better Breath Oral Health, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955630128, NDC 57955-6302-2

Batch or Lot Expiration Information

Lot# Lots: 060116G Exp. 06/19; 020817F Exp. 02/20

Recall Number: D-0771-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
180 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx PMS Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000921, NDC 57955-0095-2

Batch or Lot Expiration Information

Lot# Lots: 082316A Exp. 08/19; 022916E Exp. 02/19

Recall Number: D-0788-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
63 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Perfectionism, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, NDC UPC 357955184027, NDC 57955-1841-2

Batch or Lot Expiration Information

Lot# Lots: 042717F Exp. 04/20; 031016J Exp. 03/19

Recall Number: D-0724-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
22 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Indecision Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955277026, NDC 57955-2771-2

Batch or Lot Expiration Information

Lot# Lot: 011917L Exp. 01/20

Recall Number: D-0936-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
995 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #5 (Red Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-020118B Exp. 02/20; AUS-022418B Exp. 02/20; AUS-041718E Exp. 04/20; AUS-071718S Exp. 07/20; AUS-100117A Exp. 10/19

Recall Number: D-0960-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1110 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Advanced Arnica Super Arnica, 59 mL, Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 Imported by Ambiental Solutions, Inc. Vancouver, BC, V5Y 1E6, DIN-HM 800774305 UPC 357955181224

Batch or Lot Expiration Information

Lot# Lot: 013117P Exp. 01/20

Recall Number: D-0947-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
13198 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #12 Flu Immune Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4212-2

Batch or Lot Expiration Information

Lot# Lots: NR-010617L Exp. 01/20; NR-011216D Exp. 01/19; NR-021717G Exp. 10/19; NR-040417K Exp. 04/20; NR-061616K Exp. 06/19; NR-090115G Exp. 09/18; NR-090616K Exp. 09/19; NR-101416K Exp. 10/19; NR-120815D Exp. 12/18; NR-010318A Exp. 01/20; NR-020118N Exp. 02/20; NR-051618G Exp. 05/20

Recall Number: D-0530-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
11798 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Regional Allergies Southern U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955518426, NDC 57955-0760-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 022717K Exp. 02/20; 030816D Exp. 03/19; 030817R Exp. 03/19; 061815H Exp. 06/18; 030418A Exp. 03/20

Recall Number: D-0592-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
274 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Swollen Glands Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955512127, NDC 57955-5121-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 030216A Exp. 03/19; 100815C Exp. 10/18

Recall Number: D-0540-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
80 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Breakthrough for the Common Cold, 1 fl. oz. (29.6 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955122111, NDC 57955-1221-1

Batch or Lot Expiration Information

Lot# Lot Numbers: 031918B Exp. 03/20; 071718Z Exp. 07/20; 071818W Exp. 07/20; 071818X Exp. 07/20; 071818Y Exp. 07/20; 071818Z Exp. 07/20

Recall Number: D-0846-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
185 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Ear Relief Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955015727, NDC 57955-0154-2

Batch or Lot Expiration Information

Lot# Lots: 062215F Exp. 06/18; 091316A Exp. 09/19

Recall Number: D-0815-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
494 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx VaccinoClenz, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955003224, NDC 57955-0082-2

Batch or Lot Expiration Information

Lot# Lots: 081015F Exp. 08/18; 050216Y Exp. 05/19; 090116C Exp. 09/19

Recall Number: D-0727-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
797 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Asthma Clear Allergy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955004424, NDC 57955-0044-2

Batch or Lot Expiration Information

Lot# Lots: 012116S Exp. 01/19; 122116A Exp. 12/19

Recall Number: D-0907-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
492 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Safecare+ AllergyCare Homeopathic Non-Drowsy Taste-Free, Oral Spray, 1 fl oz (29.6 mL), UPC 357955404316, NDC 57955-4043-1

Batch or Lot Expiration Information

Lot# Lots: 021717E Exp. 02/20; 091015R Exp. 09/18

Recall Number: D-0897-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
46 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Athlete's Foot Fighter, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955012924, NDC 57955-0129-2

Batch or Lot Expiration Information

Lot# Lot: 121016A Exp. 12/19

Recall Number: D-0948-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
16495 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #2 Metal Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4202-2

Batch or Lot Expiration Information

Lot# Lots: NR-031516M Exp. 03/19; NR-073015D Exp. 09/19; NR-010617B Exp. 01/20; NR-011216M Exp. 01/19; NR-042717D Exp. 09/19; NR-051116B Exp. 05/19; NR-061616N Exp. 06/19; NR-080116E Exp. 08/19; NR-090115B Exp. 09/18; NR-090616B Exp. 09/19; NR-101416B Exp. 10/19; NR-120815R Exp. 12/18; NR-081017B Exp. 08/19; NR-020118B Exp. 02/20; NR-022318B Exp. 02/20; NR-101017B Exp. 10/19; NR-120317B Exp. 12/19

Recall Number: D-0605-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
358 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Mental Calm, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955593027, NDC 57955-5930-2

Batch or Lot Expiration Information

Lot# Lots: 080916S Exp. 08/19; 021016F Exp. 02/19; 062215J Exp. 06/18

Recall Number: D-0843-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
107 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Swollen Glands Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955012122, NDC 57955-0121-2

Batch or Lot Expiration Information

Lot# Lots: 081315L Exp. 08/18; 062415K Exp. 06/18; 120816F Exp. 12/19

Recall Number: D-0750-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Sexual Identity Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955127024, NDC 57955-1271-2

Batch or Lot Expiration Information

Lot# Lot: 021717C Exp. 02/20

Recall Number: D-0838-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
165 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CS-General Support, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955021322, NDC 57955-0213-2

Batch or Lot Expiration Information

Lot# Lots: 062716A Exp. 06/19; 091616H Exp. 09/19; 122217M Exp. 12/19

Recall Number: D-0864-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
875 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Liver Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006220, NDC 57955-0062-2

Batch or Lot Expiration Information

Lot# Lots: 073115F Exp. 07/18; 030916M Exp. 03/19; 080916W Exp. 08/19

Recall Number: D-0832-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
694 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies: Food Chemicals U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955004226, NDC 57955-0042-2

Batch or Lot Expiration Information

Lot# Lots: 062415X Exp. 06/18; 052815G Exp. 05/18; 051716T Exp. 05/19; 092216J Exp. 09/19

Recall Number: D-0652-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
182 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic AddictaPlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955508328, NDC 57955-5083-2

Batch or Lot Expiration Information

Lot# Lots: 072516B Exp. 07/19; 081715G Exp. 08/18

Recall Number: D-0859-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
137 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies: Fragrances & Phenolics, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955220022, NDC 57955-2205-2

Batch or Lot Expiration Information

Lot# Lots: 072115B Exp. 07/18; 122116B Exp. 12/19

Recall Number: D-0677-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
336 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Attention & Learning Enhancement Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955001522, NDC 57955-0015-2

Batch or Lot Expiration Information

Lot# Lots: 032316C Exp. 03/2019; 091216A Exp. 09/2019; 121617A Exp. 12/2019

Recall Number: D-0890-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
130 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx EMF Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955040026, NDC 57955-0420-2

Batch or Lot Expiration Information

Lot# Lot: 110317D Exp. 11/19

Recall Number: D-0928-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
599 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #11 (Lilac Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-072018C Exp. 07/20; AUS-100117D Exp. 10/19

Recall Number: D-0550-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
78 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Outdoor Air Pollution Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955540427, NDC 57955-6104-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 032816D Exp. 03/2019; 071116R Exp. 02/2019

Recall Number: D-0772-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
94 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CS-Rectal Bowel, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955021827, NDC 57955-0218-2

Batch or Lot Expiration Information

Lot# Lots: 022616F Exp. 02/19; 080217A Exp. 08/19; 060716K Exp. 06/19

Recall Number: D-0561-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1443 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Urinary Tract Irritations, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955505228, NDC 57955-5062-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 033116K Exp. 03/19; 060616A Exp. 06/19; 071316L Exp. 07/19; 080315G Exp. 08/18; 111516D Exp. 11/19

Recall Number: D-0770-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4648 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Candida, 8 fl. oz. (236 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955620686, NDC 57955-6207-8

Batch or Lot Expiration Information

Lot# Lots: 050216AB Exp. 05/19; 071416A Exp. 07/19; 101716C Exp. 10/19; 030117F Exp. 03/20; 120217C Exp. 12/19

Recall Number: D-0953-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
15898 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #3 Water Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4203-2

Batch or Lot Expiration Information

Lot# Lots: NR-031516L Exp. 03/19; NR-010617C Exp. 01/20; NR-011216K Exp. 01/19; NR-050916F Exp. 05/19; NR-051917A Exp. 05/20; NR-061616B Exp. 06/19; NR-080116F Exp. 08/19; NR-090115A Exp. 09/18; NR-090616C Exp. 09/19; NR-101416C Exp. 10/19; NR-120815N Exp. 12/18; NR-020118C Exp. 02/20; NR-022318C Exp. 02/20; NR-051618A Exp. 05/20; NR-071718K Exp. 07/20; NR-081017C Exp. 08/19; NR-101017C Exp. 10/19; NR-120317C Exp. 12/19

Recall Number: D-0657-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2156 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Heavy Metal Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955228127, NDC 57955-2281-2

Batch or Lot Expiration Information

Lot# Lots: 121917A Exp. 12/19

Recall Number: D-0862-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
39 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Criticize & Contradict, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955108023, NDC 57955-1081-2

Batch or Lot Expiration Information

Lot# Lot: 080315J Exp. 08/18

Recall Number: D-0762-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
289 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx TremorPlex U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955003328, NDC 57955-0033-2

Batch or Lot Expiration Information

Lot# Lots: 022516C Exp. 02/19; 072916F Exp. 07/19; 030117C Exp. 03/20

Recall Number: D-0784-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
146 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CA Miasm, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955030027, NDC 57955-0300-2

Batch or Lot Expiration Information

Lot# Lots: 033016H Exp. 03/19; 121216D Exp. 12/19

Recall Number: D-0735-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
143 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies Animal Hair & Dander Allergy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955219620, NDC 57955-2196-2

Batch or Lot Expiration Information

Lot# Lot: 020117G Exp. 02/20

Recall Number: D-0638-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
275 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Fears & Nightmares, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955509929, NDC 57955-5099-2

Batch or Lot Expiration Information

Lot# Lots: 052616F Exp. 05/19; 063015C Exp. 06/18; 102816K Exp. 10/19

Recall Number: D-0802-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
345 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Bug Away, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955007722, NDC 57955-0077-2

Batch or Lot Expiration Information

Lot# Lots: 072215C Exp. 07/18; 070516C Exp. 07/19; 050516C Exp. 05/19

Recall Number: D-0672-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
84 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine for kids! Newborn Tonic Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955511427, NDC 57955-5114-2

Batch or Lot Expiration Information

Lot# Lots: 063016K Exp. 06/2019; 112315F Exp. 11/2018

Recall Number: D-0623-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
34 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic ClaustroPlex, 2 fl. oz. (59 mL), King Bio, Inc. 3 Westside Dr. Asheville, NC 28806, UPC 357955503521, NDC 57955-5035-2

Batch or Lot Expiration Information

Lot# Lots: 021016J Exp. 02/19; 063016H Exp. 06/19

Recall Number: D-0925-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
6400 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #9 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-011117G Exp. 01/20; AUS-011916J Exp. 01/19; AUS-030816J Exp. 03/19; AUS-030917C Exp. 03/20; AUS-050516H Exp. 05/19; AUS-081516B Exp. 08/19; AUS-091515H Exp. 09/18

Recall Number: D-0589-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
430 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Varicose Veins, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955506621, NDC 57955-5566-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 030216E Exp. 03/19; 051716R Exp. 05/19; 073115G Exp. 07/18; 121216B Exp. 12/19

Recall Number: D-0860-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
198 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Environmental Adaptation: Weather Changes, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955028727, NDC 57955-0287-2

Batch or Lot Expiration Information

Lot# Lots: 072516M Exp. 07/19; 082615B Exp. 08/18

Recall Number: D-0826-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
32 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Spaced Out, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955154020, NDC 57955-1541-2

Batch or Lot Expiration Information

Lot# Lots: 052516E Exp. 05/19; 121317E Exp. 12/19

Recall Number: D-0942-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
5400 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #24 Day & Night Vitals Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4214-2

Batch or Lot Expiration Information

Lot# Lots: NR-031516B Exp. 03/19; NR-021717H Exp. 02/20; NR-050916C Exp. 05/19; NR-061616M Exp. 06/19; NR-090916A Exp. 09/19; NR-101416M Exp. 10/19; NR-120815B Exp. 12/18

Recall Number: D-0880-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
71 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Verbal Anger, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955106029, NDC 57955-1061-2

Batch or Lot Expiration Information

Lot# Lots: 082316B Exp. 08/19; 100115D Exp. 10/18

Recall Number: D-0922-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1800 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #6 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-011916F Exp. 01/19; AUS-030816F Exp. 03/19; AUS-050516F Exp. 05/19; AUS-050517F Exp. 05/20; AUS-081516D Exp. 08/19; AUS-091515E Exp. 09/18

Recall Number: D-0684-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
98 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Children's Growth & Development Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955014225, NDC 57955-0148-2

Batch or Lot Expiration Information

Lot# Lots: 020917A Exp. 02/2020; 062716E Exp. 06/2019

Recall Number: D-0800-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2747 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Appetite & Weight with P.H.A.T., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955218128, NDC 57955-2181-2

Batch or Lot Expiration Information

Lot# Lots: 072915A Exp. 07/18; 121217B Exp. 12/19; 071116Q Exp. 07/19; 102816F Exp. 10/19; 033117B Exp. 03/20

Recall Number: D-0712-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
834 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Colds & Flu Immune, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955038221, NDC 57955-0382-2

Batch or Lot Expiration Information

Lot# Lots: 063015F Exp. 06/18; 010616A Exp. 01/19; 122216B Exp. 12/19; 022417J Exp. 02/20

Recall Number: D-0973-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
100 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Melancholic Homeopathic, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955201021, NDC 57955-2011-2

Batch or Lot Expiration Information

Lot# Lots: 012317F Exp. 01/20; 051216L Exp. 05/19

Recall Number: D-0536-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
9114 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Regional Allergies Southwestern U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955518921, NDC 57955-8202-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 010118A Exp. 01/20; 020117B Exp. 02/20; 022717J Exp. 02/20; 030817N Exp. 03/19; 031417A Exp. 03/20; 041416H Exp. 04/19; 111016C Exp. 11/19; 122915C Exp. 12/18

Recall Number: D-0522-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
6446 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Lymph Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955506324, NDC 57955-5063-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 081815F Exp. 08/18; 030916V Exp. 03/19; 061316B Exp. 06/19; 1208016H Exp. 12/19; 010118BE Exp. 01/01/20; 041017M Exp. 04/19

Recall Number: D-0753-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1491 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Adrenal Burnout Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955097921, NDC 57955-0981-2

Batch or Lot Expiration Information

Lot# Lots: 021616C Exp. 02/19; 0711116P Exp. 07/19; 102816J Exp. 10/19; 030117N Exp. 03/20

Recall Number: D-0967-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3883 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Stress Control, 59 mL, (liquid/liquide), DIN-HM 80041740 UPC 357955180524

Batch or Lot Expiration Information

Lot# Lots: 011916A Exp. 01/19; 081516G Exp. 08/19

Recall Number: D-0711-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
46 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Fever Reliever Immune, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955016021, NDC 57955-0272-2

Batch or Lot Expiration Information

Lot# Lot: 010518J Exp. 01/20

Recall Number: D-0858-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
753 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Menopause Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000624, NDC 57955-0006-2

Batch or Lot Expiration Information

Lot# Lots: 072815C Exp. 07/18; 092216M Exp. 09/19

Recall Number: D-0700-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
150 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies Plains U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955260226, NDC 57955-2720-2

Batch or Lot Expiration Information

Lot# Lots: 010118E Exp. 01/20; 011917M Exp. 01/20

Recall Number: D-0633-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
66 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Additive & Preservative Detox, 2 fl. oz. (59 mL), King Bio, Inc. 3 Westside Dr. Asheville, NC 28806, UPC 357955540526, NDC 57955-6206-2

Batch or Lot Expiration Information

Lot# Lots: 051116G Exp. 05/19; 072816A Exp. 07/19

Recall Number: D-0627-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2060 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Anti-Aging & Wrinkles for Men, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955814726, NDC 57955-8147-2

Batch or Lot Expiration Information

Lot# Lots: 011916C Exp. 01/19; 072716G Exp. 07/19

Recall Number: D-0865-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
80 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies Rocky Mtns. U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955260325, NDC 57955-0062-2

Batch or Lot Expiration Information

Lot# Lot: 073115E Exp. 07/18

Recall Number: D-0841-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
225 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Hydration, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955010029, NDC 57955-0100-2

Batch or Lot Expiration Information

Lot# Lots: 062615B Exp. 06/18; 121916D Exp. 12/19; 092617E Exp. 09/19

Recall Number: D-0690-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
100 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Teething Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955001829, NDC 57955-0018-2

Batch or Lot Expiration Information

Lot# Lots: 032216C Exp. 03/19

Recall Number: D-0650-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
31 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Mood Changes, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955503729, NDC 57955-5037-2

Batch or Lot Expiration Information

Lot# Lots: 062816D Exp. 06/19

Recall Number: D-0528-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
6210 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Regional Allergies Pacific U.S. 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955519324, NDC 57955-8198-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 030816C Exp. 03/19; 052616C Exp. 05/19; 062215K Exp. 06/18; 012518B Exp. 01/20; 040218B Exp. 04/20; 050417A Exp. 05/19; 030817P Exp. 03/19

Recall Number: D-0877-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
90 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Hangover Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955011323, NDC 57955-0113-2

Batch or Lot Expiration Information

Lot# Lots: 083115A Exp. 08/18; 091416E Exp. 09/19

Recall Number: D-0680-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
53 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Lonely Mind & Body High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955200024, NDC 57955-2001-2

Batch or Lot Expiration Information

Lot# Lots: 010518H Exp. 01/20; 040616N Exp. 04/19

Recall Number: D-0985-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
162 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Breast Cyst & Discomforts High Potency Homeopathic Formula for Professional Use Only, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955000327, NDC 57955-0003-2

Batch or Lot Expiration Information

Lot# Lots: 040616B Exp. 04/19; 020917G Exp. 02/20

Recall Number: D-0776-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
98 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CS-Breast, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955021421, NDC 57955-0214-2

Batch or Lot Expiration Information

Lot# Lots: 091515A Exp. 09/18; 010517B Exp. 01/20

Recall Number: D-0834-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
133 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Acid Clenz, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955012726, NDC 57955-0127-2

Batch or Lot Expiration Information

Lot# Lots: 050216U Exp. 05/19; 072716C Exp. 07/19

Recall Number: D-0875-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
292 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Water Retention Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955027829, NDC 57955-0278-2

Batch or Lot Expiration Information

Lot# Lot: 081015E Exp. 08/18

Recall Number: D-0667-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1083 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine for kids! Attention & Learning Enhancement Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955501527, NDC 57955-5015-2

Batch or Lot Expiration Information

Lot# Lots: 050216G Exp. 05/2016; 070816C Exp. 07/2019; 092617F Exp. 09/2019

Recall Number: D-0660-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
12127 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Aquaflora Kids Candida Relief Homeopathic, 4 fl. oz. (118 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955332244

Batch or Lot Expiration Information

Lot# Lots: 011416G Exp. 12/2019; 011917R Exp. 01/2020; 041518H Exp. 09/2018; 081016E Exp. 08/2019; 092815AA Exp. 09/2018

Recall Number: D-0646-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
322 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Acid Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955512721, NDC 57955-5227-2

Batch or Lot Expiration Information

Lot# Lots: 060716A Exp. 06/19; 092216H Exp. 09/19

Recall Number: D-0758-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
14 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Chagrined, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955204022, NDC 57955-2041-2

Batch or Lot Expiration Information

Lot# Lots: 060616D Exp. 06/19; 022117H Exp. 02/20

Recall Number: D-0748-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
96 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Fears & Nightmares Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955181026, NDC 57955-1811-2

Batch or Lot Expiration Information

Lot# Lots: 071116C Exp. 07/19; 022017C Exp. 02/20

Recall Number: D-0552-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2898 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic 9-1-1 Burnout, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955597926, NDC 57955-5979-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 032816F Exp. 03/19; 060816C Exp. 03/19; 082916A Exp. 08/19

Recall Number: D-0945-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
19490 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #5 Fire Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4205-2

Batch or Lot Expiration Information

Lot# Lots: NR-022318E Exp. 02/20; NR-030418A Exp. 03/20; NR-051618D Exp. 05/20; NR-051818D Exp. 05/20; NR-081017E Exp. 08/19; NR-120317E Exp. 12/19; NR-121517A Exp. 12/19; NR-031516J Exp. 3/19; NR-010617E Exp. 01/20; NR011216H Exp. 01/19; NR-040417C Exp. 4/20; NR-050916D Exp. 5/19; NR-061517A Exp. 6/20; NR-061616D Exp. 6/19; NR-080116A Exp. 8/19; NR090115J Exp. 9/18; NR-090916B Exp. 9/19; NR-101416E Exp. 10/19; NR-120815K Exp.12/18

Recall Number: D-0713-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2644 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Stress Control Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955185024, NDC 57955-1852-2

Batch or Lot Expiration Information

Lot# Lots: 072115A Exp. 07/18; 010616C Exp. 01/19; 021216G Exp. 02/19; 072516C Exp. 07/19; 101817A Exp. 10/19; 030818H Exp. 03/20

Recall Number: D-0564-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
309 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Hangover Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955511328, NDC 57955-5113-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 033116Q Exp. 03/19; 083115C Exp. 08/18; 111516E Exp. 11/19

Recall Number: D-0763-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1002 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Chronic Viro Reliever U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955008828, NDC 57955-0103-2

Batch or Lot Expiration Information

Lot# Lots: 080916C Exp. 08/19; 022618A Exp. 02/20; 072115F Exp. 07/18; 022516B Exp. 02/19; 052616N Exp. 05/19

Recall Number: D-0984-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
48 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Aversion to Change High Potency Homeopathic Formula for Professional Use Only, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955280026, NDC 57955-2800-2

Batch or Lot Expiration Information

Lot# Lots: 072015H Exp. 07/18; 111016E Exp. 11/19; 011917N Exp. 01/20

Recall Number: D-0842-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
102 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx AddictaPlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955300021, NDC 57955-3003-2

Batch or Lot Expiration Information

Lot# Lot: 062415R Exp. 06/18

Recall Number: D-0861-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
288 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergy & Red Eye Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955016427, NDC 57955-0164-2

Batch or Lot Expiration Information

Lot# Lots: 072816B Exp. 07/19; 080315B Exp. 08/18

Recall Number: D-0792-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
544 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Artery/Cholesterol/BP, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006428, NDC 57955-0064-2

Batch or Lot Expiration Information

Lot# Lots: 092915G Exp. 09/18; 041416F Exp. 04/19

Recall Number: D-0614-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1326 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Food Chemical Intolerances, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955504221, NDC 57955-0728-2

Batch or Lot Expiration Information

Lot# Lots: 120516A Exp. 12/19; 060316C Exp. 06/19; 010118S Exp. 01/20

Recall Number: D-0659-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
600 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Kids Bed Wetting Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955501220, NDC 57955-0447-2

Batch or Lot Expiration Information

Lot# Lots: 101615B Exp. 10/2018; 111717C Exp. 11/2019

Recall Number: D-0560-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2433 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Yeast Freee, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955507628, NDC 57955-5076-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 011518E Exp. 01/20; 033116J Exp. 03/19; 041017C Exp. 04/19; 072216G Exp. 07/19

Recall Number: D-0798-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
600 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Grief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955206026, NDC 57955-2061-2

Batch or Lot Expiration Information

Lot# Lots: 062415M Exp. 06/18; 040616P Exp. 04/19; 102016K Exp. 10/19

Recall Number: D-0542-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1735 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Gallbladder Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955506829, NDC 57955-6058-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 031017K Exp. 03/20; 040616E Exp. 04/19; 060216F Exp. 06/19

Recall Number: D-0604-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
10025 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Multi-Strain Flu Relief, 2 fl. oz. (59 mL), King Bio, Inc. 3 Westside Dr. Asheville, NC 28806, UPC 357955519928, NDC 57955-5194-2

Batch or Lot Expiration Information

Lot# Lots: 013018A Exp. 01/2020; 020618B Exp. 02/20; 072716H Exp. 07/19; 120617A Exp. 12/2019

Recall Number: D-0681-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
40 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Colic Relief Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955015826, NDC 57955-0178-2

Batch or Lot Expiration Information

Lot# Lots: 111717E Exp. 11/19

Recall Number: D-0699-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
17527 tubes

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Soothing Advanced Arnica Pure Homeopathic Cream, 3 oz. (85 g), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955400035, NDC 57955-4000-3

Batch or Lot Expiration Information

Lot# Lots: 052616 Exp. 05/19; 073118ZZ Exp. 07/21; 040117ZZ Exp. 06/19; 122717ZZ Exp. 12/20; 040417ZZ Exp. 04/20; 091617ZZ Exp. 09/20

Recall Number: D-0640-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
500 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Ileocecal Valve Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955509820, NDC 57955-6083-2

Batch or Lot Expiration Information

Lot# Lots: 060116E Exp. 06/19; 083017F Exp. 08/19; 101716E Exp. 10/19

Recall Number: D-0952-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
14695 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #11 Visceral Polarity Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4211-2

Batch or Lot Expiration Information

Lot# Lots: NR-031516D Exp. 03/19; NR-073015H Exp. 07/18; NR-010617K Exp. 01/20; NR-011216A Exp. 01/19; NR-050916B Exp. 05/19; NR-061616J Exp. 06/19; NR-080116J Exp. 08/19; NR-090115D Exp. 09/18; NR-090816A Exp. 09/19; NR-101416J Exp. 10/19; NR-120815F Exp. 12/18; NR-020118M Exp. 02/20; NR-072617A Exp. 07/19; NR-110117C Exp. 11/19; NR-120317L Exp. 12/19

Recall Number: D-0881-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
13 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Shy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955275022, NDC 57955-2751-2

Batch or Lot Expiration Information

Lot# Lot: 091616F Exp. 09/19

Recall Number: D-0879-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
45 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies: Nightshades, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955250029, NDC 57955-2502-2

Batch or Lot Expiration Information

Lot# Lot: 082316C Exp. 08/19

Recall Number: D-0556-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
21925 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Anxiety & Nervousness, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955516323, NDC 57955-5163-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 033116D Exp. 03/19; 042717D Exp. 04/20; 061616A Exp. 06/19; 072818A Exp. 07/20; 081015D Exp. 08/18; 091516C Exp. 09/19; 112117F Exp. 11/19; 121516A Exp. 12/19

Recall Number: D-0721-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
165 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies: Dust Mite & Roach Allergy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955219729, NDC 57955-2197-2

Batch or Lot Expiration Information

Lot# Lots: 062816G Exp. 06/19; 011617B Exp. 01/20

Recall Number: D-0775-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
18 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CS-Bone, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955021124, NDC 57955-0211-2

Batch or Lot Expiration Information

Lot# Lot: 011617C Exp. 01/20

Recall Number: D-0658-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3412 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Kids Teething Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955501824, NDC 57955-0527-2

Batch or Lot Expiration Information

Lot# Lots: 020118F Exp. 02/2020; 020717B Exp. 02/2020; 080317D Exp. 08/2019; 110716C Exp. 11/2019; 111617E Exp. 11/2019

Recall Number: D-0617-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
146 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Dust Mite & Roach Allergy Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955519720, NDC 57955-6497-2

Batch or Lot Expiration Information

Lot# Lots: 020917L Exp. 02/20; 051116F Exp. 05/19; 100416A Exp. 10/19

Recall Number: D-0904-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2086 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Aquaflora Heavy Metal Detox Candida, 2 fl. oz. (59 mL), Homeopathic, King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 USA, NDC 57955-2281-2

Batch or Lot Expiration Information

Lot# Lot: 080216A Exp. 08/19

Recall Number: D-0565-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
158 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Weather Changes, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955528722, NDC 57955-5287-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 033116R Exp. 03/19; 070816A Exp. 07/19

Recall Number: D-0886-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
95 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx GynePlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000723, NDC 57955-0007-2

Batch or Lot Expiration Information

Lot# Lots: 091015F Exp. 09/18; 100416C Exp. 10/19

Recall Number: D-0738-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1530 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Acute Viro Reliever, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955008125, NDC 57955-0432-2

Batch or Lot Expiration Information

Lot# Lots: 101617D Exp. 10/19; 072815F Exp. 07/18; 031016L Exp. 03/19; 020618A Exp. 02/20

Recall Number: D-0898-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
26 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CS-Ovary, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955021629, NDC 57955-0216-2

Batch or Lot Expiration Information

Lot# Lots: 123115A Exp. 12/18; 122216J Exp. 12/19

Recall Number: D-0909-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
190189 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Safecare+ AsthmaCare Homeopathic, Not a Rescue Inhaler, 2 fl oz (59 mL), UPC 357955404422, NDC 57955-4044-1

Batch or Lot Expiration Information

Lot# Lots: 122216K Exp. 12/19; 120217P Exp. 12/19; 111117C Exp. 11/19; 083116C Exp. 08/19; 082316E Exp. 08/19; 072015A Exp. 07/18; 062716C Exp. 06/19; 062316B Exp. 06/19; 062218C Exp. 06/20; 052218C Exp. 05/20; 052118C Exp. 05/20; 051716J Exp. 05/19; 041816C Exp. 04/19; 030316A Exp. 03/19; 022317H Exp. 02/20; 111516H Exp. 11/19; 091815A Exp. 09/18; 062718C Exp. 06/20; 081815A Exp. 08/18

Recall Number: D-0955-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
5092 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #25 Yin/Yang Balance Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4215-2

Batch or Lot Expiration Information

Lot# Lots: NR-031516A Exp. 03/19; NR-042717B Exp. 04/20; NR-090616N Exp. 09/19; NR-100115A Exp. 10/18; NR-120815E Exp. 12/18; NR-020118T Exp. 10/19; NR-022318L Exp. 02/20; NR-022318P Exp. 10/19; NR-092717A Exp. 09/19

Recall Number: D-0744-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
386 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Heart Regularity Circulation, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006527, NDC 57955-0065-2

Batch or Lot Expiration Information

Lot# Lots: 083115F Exp. 08/18; 091516D Exp. 09/19; 020917K Exp. 02/20

Recall Number: D-0831-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
97 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies: Nuts & Seeds, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955220428, NDC 57955-2204-2

Batch or Lot Expiration Information

Lot# Lots: 082815A Exp. 08/18; 112117D Exp. 11/19; 061416A Exp. 06/19

Recall Number: D-0632-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
16 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Dental Plak, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955887027, NDC 57955-1904-2

Batch or Lot Expiration Information

Lot# Lots: 051116E Exp. 05/19

Recall Number: D-0572-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1018 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic PMS Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955500926, NDC 57955-5009-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 050216J Exp. 05/19; 080416C Exp. 08/19; 081815K Exp. 08/18

Recall Number: D-0562-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
367 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Animal Hair & Dander Allergy Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955519621, NDC 57955-6490-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 012616J Exp. 01/19; 033116L Exp. 03/19

Recall Number: D-0963-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
981 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Anxiety & Nervousness, 59 mL, (liquid/liquide), DIN-HM 80074778 UPC 357955181521

Batch or Lot Expiration Information

Lot# Lots: 060917B Exp. 06/20; 021517J Exp. 02/20

Recall Number: D-0682-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Children's Appetite & Weight Control Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955251729, NDC 57955-2518-2

Batch or Lot Expiration Information

Lot# Lots: 102016J Exp. 10/19

Recall Number: D-0673-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2404 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Kids Sleep Aid Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955042426, NDC 57955-0424-2

Batch or Lot Expiration Information

Lot# Lots: 063016D Exp. 06/2019; 081016F Exp. 08/2019

Recall Number: D-0804-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
194 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Indigestion Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955002420, NDC 57955-0024-2

Batch or Lot Expiration Information

Lot# Lot: 041416M Exp. 04/19

Recall Number: D-0979-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
97 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCareRx CS-Lung High Potency Homeopathic Formula for Professional Use Only, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955022626, NDC 57955-0226-2

Batch or Lot Expiration Information

Lot# Lots: 052516M Exp. 05/19; 052815E Exp. 05/18

Recall Number: D-0900-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
5000 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Aquaflora High Potency Candida Control Program Homeopathic Formula, Net 16 fl. oz. (1 pt) 473 mL, Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955160366, NDC 57955-1603-6

Batch or Lot Expiration Information

Lot# Lots: 011017A Exp. 01/20; 033116T Exp. 03/19; 052516R Exp. 05/19; 122815A Exp. 12/18

Recall Number: D-0814-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
15 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Dental Plak, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955008620, NDC 57955-0086-2

Batch or Lot Expiration Information

Lot# Lots: 051116C Exp. 05/19; 110916C Exp. 11/19

Recall Number: D-0686-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
15 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Newborn Tonic Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955011422, NDC 57955-0114-2

Batch or Lot Expiration Information

Lot# Lots: 110915H Exp. 11/18

Recall Number: D-0725-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
48 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Aversion to Change Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955280026, NDC 57955-2800-2

Batch or Lot Expiration Information

Lot# Lots: 072015H Exp. 07/18; 111016F Exp. 11/19; 011917N Exp. 01/20

Recall Number: D-0597-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2078 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Smoke Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955508021, NDC 57955-5080-2

Batch or Lot Expiration Information

Lot# Lots: 012017C Exp. 01/20; 022618B Exp. 02/20; 063016A Exp. 06/19

Recall Number: D-0668-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
205 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine for kids! Children's Ear Relief Formula Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955531524, NDC 57955-0416-2

Batch or Lot Expiration Information

Lot# Lots: 050216P Exp. 05/2019; 072516G Exp. 07/2019; 112315B Exp. 11/2018

Recall Number: D-0968-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3384 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Respiratory Care, 59 mL, (liquid/liquide), DIN-HM 80035323 UPC 357955180623

Batch or Lot Expiration Information

Lot# Lots: 011516B Exp. 01/19; 082216B Exp. 08/19

Recall Number: D-0723-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
288 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx SciatiPlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955003021, NDC 57955-0030-2

Batch or Lot Expiration Information

Lot# Lots: 011817D Exp. 01/20; 080315D Exp. 08/18

Recall Number: D-0941-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
23000 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #8 Allergy Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4208-2

Batch or Lot Expiration Information

Lot# Lots: NR-031516F Exp. 03/19; NR-073015E Exp. 07/18; NR-010617F Exp. 01/20; NR-011216F Exp. 01/19; NR-021717E Exp. 02/20; NR-051116C Exp. 05/19; NR-060517B Exp. 06/20; NR-061616G Exp. 06/19; NR-080116C Exp. 08/19; NR-090115E Exp. 09/18; NR-090616G Exp. 09/19; NR-101916A Exp. 10/19; NR-120815J Exp. 12/18

Recall Number: D-0807-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1012 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Lungs & Bronchial Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955005322, NDC 57955-0053-2

Batch or Lot Expiration Information

Lot# Lots: 070816B Exp. 07/19; 080917A Exp. 08/19; 050216N Exp. 05/19

Recall Number: D-0587-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
153 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Breast Inflammations & Discomforts, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955500322, NDC 57955-5003-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 040616D Exp. 04/19; 081016C Exp. 08/19; 010518K Exp. 01/20

Recall Number: D-0675-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
149 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine for kids! Children's Appetite & Weight Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955551720, NDC 57955-6017-2

Batch or Lot Expiration Information

Lot# Lots: 102016J Exp. 10/19; 080916M Exp. 08/2019; 091316D Exp. 09/2019

Recall Number: D-0894-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
39 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx PSOR Miasm, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955030126, NDC 57955-0307-2

Batch or Lot Expiration Information

Lot# Lot: 120217D Exp. 12/19

Recall Number: D-0854-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
153 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Heartache, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955203025, NDC 57955-2030-2

Batch or Lot Expiration Information

Lot# Lots: 082015A Exp. 08/18; 072516F Exp. 07/19

Recall Number: D-0585-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
360 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Grains & Gluten Intolerances, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955520429, NDC 57955-0724-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 012517G Exp. 01/20; 040716A Exp. 04/19; 052516Z Exp. 05/19

Recall Number: D-0645-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
295 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Prostate Symptom Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955501121, NDC 57955-0241-2

Batch or Lot Expiration Information

Lot# Lots: 060616B Exp. 06/19

Recall Number: D-0872-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
94 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Muscle Maximizer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955013327, NDC 57955-0133-2

Batch or Lot Expiration Information

Lot# Lot: 081616C Exp. 08/19

Recall Number: D-0543-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
5080 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Restless Leg Symptom Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955544524, NDC 57955-6235-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 031218D Exp. 03/20; 042717C Exp. 04/20; 072815A Exp. 07/18; 092216C Exp. 09/19; 120217E Exp. 12/19

Recall Number: D-0931-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
600 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #20 (Red, White and Blue Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lot: AUS-031618A Exp. 03/20; AUS-111317A Exp. 11/19; AUS-121717C Exp. 12/19

Recall Number: D-0631-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
237 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Fears & Phobias, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955515227, NDC 57955-5152-2

Batch or Lot Expiration Information

Lot# Lots: 050916G Exp. 05/19; 120816L Exp. 12/19

Recall Number: D-0801-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
10 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Expressed Sexual Issues, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955125020, NDC 57955-1257-2

Batch or Lot Expiration Information

Lot# Lot: 051216M Exp. 05/19

Recall Number: D-0569-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
124 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Indoor Air Pollution Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955540120, NDC 57955-6001-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 050216Q Exp. 05/19; 063016J Exp. 06/19

Recall Number: D-0805-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
245 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx VeinoPlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006626, NDC 57955-0066-2

Batch or Lot Expiration Information

Lot# Lots: 062415H Exp. 06/18; 111516P Exp. 11/19; 062016D Exp. 06/19; 040717D Exp. 04/19

Recall Number: D-0644-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
89 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Birth Ease, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955500223, NDC 57955-5002-2

Batch or Lot Expiration Information

Lot# Lots: 060316D Exp. 06/19

Recall Number: D-0916-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1300 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #20 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-011916N Exp. 01/19; AUS-050516K Exp. 05/19; AUS-091515J Exp. 09/18; AUS-101416A Exp. 10/19

Recall Number: D-0701-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
19 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CS-Uterus Cancer Support, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955022121, NDC 57955-0247-2

Batch or Lot Expiration Information

Lot# Lots: 092216D Exp. 09/19; 010118H Exp. 01/20

Recall Number: D-0584-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
452 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Morning Sickness Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955500827, NDC 57955-6008-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 040616K Exp. 04/2019; 072716J Exp. 07/2019

Recall Number: D-0813-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
15 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Reserved, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955228028, NDC 57955-2282-2

Batch or Lot Expiration Information

Lot# Lot: 051216P Exp. 05/19

Recall Number: D-0766-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1329 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies: Mold, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955650126, NDC 57955-6501-2

Batch or Lot Expiration Information

Lot# Lots: 072015D Exp. 07/18; 022317F Exp. 02/20; 123015B Exp. 12/18; 062816B Exp. 06/19; 091616B Exp. 09/19

Recall Number: D-0709-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
24 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx UlcerPlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955175025, NDC 57955-0188-2

Batch or Lot Expiration Information

Lot# Lot: 010418D Exp. 01/20

Recall Number: D-0539-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1753 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Colds & Flu Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955518228, NDC 57955-6182-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 010615B Exp. 01/19; 030916U Exp. 03/19; 121117D Exp. 12/19

Recall Number: D-0607-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1046 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Headache Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955515326, NDC 57955-5153-2

Batch or Lot Expiration Information

Lot# Lots: 020718B Exp. 02/20; 091616M Exp. 09/19

Recall Number: D-0983-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
194 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Regional Allergies Hawaii U.S. Homeopathic, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955520620, NDC 57955-5206-2

Batch or Lot Expiration Information

Lot# Lots: 050216M Exp. 05/19; 070516A Exp. 07/19

Recall Number: D-0871-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
81 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx ApoPlex, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006725, NDC 57955-0067-2

Batch or Lot Expiration Information

Lot# Lots: 081715F Exp. 08/18; 091616J Exp. 09/19

Recall Number: D-0600-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
14978 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Sciatic Nerve Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955503026, NDC 57955-6030-2

Batch or Lot Expiration Information

Lot# Lots: 012116B Exp. 01/19; 012317E Exp. 01/20; 052516S Exp. 05/19; 071315A Exp. 07/18; 071818E Exp. 07/20; 080917B Exp. 08/19; 091416F Exp. 09/19; 120217A Exp. 12/19

Recall Number: D-0639-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
479 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Indigestion Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955502425, NDC 57955-5024-2

Batch or Lot Expiration Information

Lot# Lots: 052616G Exp. 05/19; 080315C Exp. 08/18; 123016D Exp. 12/19

Recall Number: D-0545-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1520 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Constipation Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955501923, NDC 57955-5019-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 031517B Exp. 03/20; 040616G Exp. 04/19; 072716B Exp. 07/19

Recall Number: D-0602-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
181 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic No Sweat Anti-Perspirant, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955508526, NDC 57955-5085-2

Batch or Lot Expiration Information

Lot# Lots: 012616E Exp. 01/2019; 060716B Exp. 06/19

Recall Number: D-0977-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1807 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Bronchial Care, 59 mL (liquid/liquid), Manufactured by: King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 Imported by Ambiental Solutions, Inc. Vancouver, BC, V5Y 1E6, DIN-HM 80035774 UPC 357955180425

Batch or Lot Expiration Information

Lot# Lot: 110416A Exp. 11/19

Recall Number: D-0685-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
165 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Children's Cough Children High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955014522, NDC 57955-0145-2

Batch or Lot Expiration Information

Lot# Lots: 091015B Exp. 09/2018; 120616B Exp. 12/2019

Recall Number: D-0731-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
85 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx SYP Miasm Constitution, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955030324, NDC 57955-0306-2

Batch or Lot Expiration Information

Lot# Lots: 012517H Exp. 01/20; 081015N Exp. 08/18

Recall Number: D-0852-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
20 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx No Sweat/Anti-Perspirant, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955008521, NDC 57955-0085-2

Batch or Lot Expiration Information

Lot# Lot: 063016E Exp. 06/19

Recall Number: D-0557-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
11055 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Advanced Arnica, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955598428, NDC 57955-5984-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 010518D Exp. 01/20; 033116E Exp. 03/19; 080916H Exp. 08/19; 080917C Exp. 08/2019; 081015C Exp. 08/18

Recall Number: D-0535-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
4499 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Regional Allergies Great Lakes U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955519027, NDC 57955-8195-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 030817K Exp. 03/19; 030916H Exp. 03/19; 061615F Exp. 06/18; 071416B Exp. 07/19; 022618J Exp. 02/20

Recall Number: D-0571-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2045 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Hemorrhoid Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955502326, NDC 57955-5023-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 012317C Exp. 01/20; 052516U Exp. 05/19; 050216S Exp. 05/19

Recall Number: D-0531-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
478 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Heart Regularity, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955506522, NDC 57955-5065-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 030718F Exp. 03/20; 051716N Exp. 05/19; 080916K Exp. 08/19

Recall Number: D-0575-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
18707 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Asthma Symptom Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955504429, NDC 57955-6044-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 022117B Exp. 02/20; 042417B Exp. 04/20; 050118M Exp. 05/20; 052516X Exp. 05/19; 062215B Exp. 06/18; 091015S Exp. 09/18; 091416H Exp. 09/19; 101017E Exp. 10/19

Recall Number: D-0911-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2600 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #1 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-091515A Exp. 09/18; AUS-081516H Exp. 08/19; AUS-050516A Exp. 05/19; AUS-030816A Exp. 03/19; AUS-011117A Exp. 01/20; AUS-011916A Exp. 01/19

Recall Number: D-0524-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3651 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Regional Allergies Northeastern U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955519225, NDC 57955-0753-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 030817M Exp. 03/19; 050216E Exp. 05/19; 070816D Exp. 07/19; 010118D Exp. 01/20; 030418B Exp. 03/20

Recall Number: D-0647-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
19 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Caffeine Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955540229, NDC 57955-6202-2

Batch or Lot Expiration Information

Lot# Lots: 062415T Exp. 06/18; 092716B Exp. 09/19

Recall Number: D-0752-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
101 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Sluggish Mind Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955152026, NDC 57955-1521-2

Batch or Lot Expiration Information

Lot# Lots: 021616F Exp. 02/19; 111416A Exp. 11/19

Recall Number: D-0624-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
349 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Bug Away, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955507727, NDC 57955-5077-2

Batch or Lot Expiration Information

Lot# Lots: 020116A Exp. 07/19; 050516B Exp. 05/19; 071116B Exp. 07/19

Recall Number: D-0756-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
25 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Environmental Adaptation Cold/Damp, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955028420, NDC 57955-0284-2

Batch or Lot Expiration Information

Lot# Lots: 022316A Exp. 02/19; 031517A Exp. 03/20

Recall Number: D-0596-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
6028 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Sore Throat & Laryngitis, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955505822, NDC 57955-5058-2

Batch or Lot Expiration Information

Lot# Lots: 010118AH Exp. 01/20; 020916R Exp. 02/19; 022017B Exp. 02/20; 080415E Exp. 08/18; 090816F Exp. 09/19

Recall Number: D-0870-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
57 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Aller-Detox: Indoor Pollution Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955240129, NDC 57955-2408-2

Batch or Lot Expiration Information

Lot# Lot: 080415F Exp. 08/18

Recall Number: D-0972-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
98 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Aller-Detox: Outdoor Pollution Control Homeopathic, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955240426, NDC 57955-2404-2

Batch or Lot Expiration Information

Lot# Lots: 070815C Exp. 07/18; 070116A Exp. 06/19

Recall Number: D-0777-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
340 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Sore Throat & Laryngitis, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955005827, NDC 57955-0137-2

Batch or Lot Expiration Information

Lot# Lots: 072815M Exp. 07/18; 031016K Exp. 03/19; 030718H Exp. 03/20

Recall Number: D-0903-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2634 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Aquaflora Enzyme Restoration Upper GI Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955232124, NDC 57955-3321-2

Batch or Lot Expiration Information

Lot# Lots: 102016H Exp. 10/19; 010518E Exp. 01/20; 050616A Exp. 05/19

Recall Number: D-0615-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
285 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Fever Reliever, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955516026, NDC 57955-5160-2

Batch or Lot Expiration Information

Lot# Lots: 022417H Exp. 02/20; 030216D Exp. 03/19; 052616J Exp. 05/19; 092815B Exp. 09/18

Recall Number: D-0674-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3271 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Kids Multi-Strain Flu Relief Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955042228, NDC 57955-0422-2

Batch or Lot Expiration Information

Lot# Lots: 071316A Exp. 07/2019; 111015B Exp. 11/2018; 112015A Exp. 11/2018

Recall Number: D-0595-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
51 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Sporting Edge, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955503125, NDC 57955-5031-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 010118AF Exp. 01/20; 022916D Exp. 02/19

Recall Number: D-0895-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
15 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Foul Bowel, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955031925, NDC 57955-0319-2

Batch or Lot Expiration Information

Lot# Lot: 120516C Exp. 11/19

Recall Number: D-0749-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
783 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Cold Sores & Herpes Skin, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955016526, NDC 57955-0165-2

Batch or Lot Expiration Information

Lot# Lots: 032216D Exp. 03/19; 072815G Exp. 07/18; 022017A Exp. 02/20

Recall Number: D-0970-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
352 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Appetite Enhancer Homeopathic, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955512820

Batch or Lot Expiration Information

Lot# Lot: 121117E Exp. 12/19

Recall Number: D-0590-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1999 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Total Mold Allergy Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955519522, NDC 57955-6287-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 020916A Exp. 02/19; 080916P Exp. 08/19; 081315M Exp. 08/18

Recall Number: D-0932-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
695 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #24 (Blue, White and Purple Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lot: AUS-100117H Exp. 10/19; AUS-020118J Exp. 02/20; AUS-041618C Exp. 02/20

Recall Number: D-0732-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
154 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Anti-Aging & Wrinkles For Men, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955714729, NDC 57955-7148-2

Batch or Lot Expiration Information

Lot# Lots: 012517J Exp. 01/20; 021616D Exp. 02/19; 051716V Exp. 05/19

Recall Number: D-0908-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
14380 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Safecare+ AsthmaCare Homeopathic, Not a Rescue Inhaler, 1 fl oz (29.6 mL), UPC 357955704416, NDC 57955-7044-1

Batch or Lot Expiration Information

Lot# Lots: 030316B Exp. 03/19; 061715A Exp. 06/18; 061715B Exp. 06/18

Recall Number: D-0618-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2108 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Diarrhea Relief, 2 fl. oz. (59 mL), King Bio, Inc. 3 Westside Dr. Asheville, NC 28806, UPC 357955502029, NDC 57955-5020-2

Batch or Lot Expiration Information

Lot# Lots: 020916Q Exp. 02/19; 022117C Exp. 02/20; 072015C Exp. 07/18; 081816D Exp. 08/19

Recall Number: D-0534-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
5984 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Regional Allergies Desert U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955518822, NDC 57955-8196-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 030916Q Exp. 03/19; 052616A Exp. 05/19; 072516J Exp. 07/19; 072815B Exp. 07/18; 012918A Exp. 01/20; 030817J Exp. 03/19

Recall Number: D-0741-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1045 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergy/Hay Fever Reliever Allergy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955004325, NDC 57955-0043-2

Batch or Lot Expiration Information

Lot# Lots: 052616F Exp. 05/19; 020917B Exp. 02/20; 030718D Exp. 03/20

Recall Number: D-0949-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
14249 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #20 Pain Relief Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4213-2

Batch or Lot Expiration Information

Lot# Lots: NR-010617M Exp. 01/20; NR-031516C Exp. 03/19; NR-061616L Exp. 06/19; NR-090115F Exp. 09/18; NR-090616M Exp. 09/19; NR-101416L Exp. 10/19; NR-120815C Exp. 12/18; NR-020118P Exp. 02/20; NR-022318K Exp. 02/20; NR-022318M Exp. 02/20; NR-052517A Exp. 05/20; NR-060517F Exp. 06/20; NR-060618A Exp. 06/20; NR-061418A Exp. 06/20; NR-121417B Exp. 12/19

Recall Number: D-0964-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
957 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Regional Allergies Eastern Canada, 59 mL, (liquid/liquide) DIN-HM 80075212 UPC 357955181620

Batch or Lot Expiration Information

Lot# Lots: 060917E Exp. 06/20; 021517K Exp. 02/20

Recall Number: D-0889-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
441 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Poison Ivy & Oak Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955011620, NDC 57955-0116-2

Batch or Lot Expiration Information

Lot# Lots: 091015L Exp. 09/18; 092216F Exp. 09/19

Recall Number: D-0570-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
7783 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Anti-Aging & Wrinkles for Women, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955814825, NDC 57955-8148-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 010518L Exp. 01/20; 020718A Exp. 02/20; 050216R Exp. 05/19; 081815H Exp. 08/18; 101116C Exp. 10/19

Recall Number: D-0821-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
186 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Obsessions/Compulsions, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955183020, NDC 57955-1831-2

Batch or Lot Expiration Information

Lot# Lots: 060116F Exp. 06/19; 020917F Exp. 02/20

Recall Number: D-0705-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1927 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Lymph Detox Cleansing & Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 35795506329, NDC 57955-0339-2

Batch or Lot Expiration Information

Lot# Lots: 080315A Exp. 08/18; 030916K Exp. 03/19; 080916T Exp. 08/19; 020817G Exp. 02/20; 010118V Exp. 01/20

Recall Number: D-0654-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1069 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Poison Ivy & Oak Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955511625, NDC 57955-5116-2

Batch or Lot Expiration Information

Lot# Lots: 080216B Exp. 08/19; 121417J Exp. 12/19

Recall Number: D-0625-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
17 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Better Breath, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955880127

Batch or Lot Expiration Information

Lot# Lots: 010118F Exp. 01/20; 051716E Exp. 05/19

Recall Number: D-0761-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
438 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Headache Freee... U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955015321 NDC 57955-0153-2

Batch or Lot Expiration Information

Lot# Lots: 022516D Exp. 02/19; 080916A Exp. 08/19; 121317K Exp. 12/19

Recall Number: D-0905-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
3840 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Aquaflora Probiotic Restoration Lower GI Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955232025, NDC 57955-3320-2

Batch or Lot Expiration Information

Lot# Lots: 020618D Exp. 02/20; 030916P Exp. 03/19; 041215I Exp. 04/18; 072216L Exp. 07/19

Recall Number: D-0914-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
2100 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #12 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-101116C Exp. 10/19; AUS-050916A Exp. 05/19; AUS-030917E Exp. 03/20; AUS-011916M Exp. 01/19; AUS091515K Exp. 09/18; AUS-030816L Exp. 03/19

Recall Number: D-0899-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1969 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
People's Best Arnica Gel Homeopathic Medicine Pain Relief, Net Wt. 2.6 oz (73 g), www.kingbio.com, UPC 357955320326, NDC 57955-3203-3

Batch or Lot Expiration Information

Lot# Lots: 111617ZZ Exp. 11/19; 072016ZZ Exp. 07/18; 092316ZZ Exp. 09/18

Recall Number: D-0863-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
85 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx CS-Lymph Hodgkins, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955021520, NDC 57955-0215-2

Batch or Lot Expiration Information

Lot# Lots: 080315F Exp. 08/18; 121916B Exp. 12/19

Recall Number: D-0580-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
38 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Hydration, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955024224, NDC 57955-0242-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 041816A Exp. 04/19; 070816E Exp. 07/19

Recall Number: D-0787-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
896 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Heavy Metal Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955028123, NDC 57955-0281-2

Batch or Lot Expiration Information

Lot# Lots: 090816H Exp. 09/19; 072815D Exp. 07/18; 031017J Exp. 03/20

Recall Number: D-0935-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1200 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #4 (Green Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-071718R Exp. 07/20; AUS-110117A Exp. 11/19

Recall Number: D-0892-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
12 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Neglectful, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955255024, NDC 57955-2551-2

Batch or Lot Expiration Information

Lot# Lot: 112916A Exp. 11/19

Recall Number: D-0958-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
20098 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #9 ER 911 Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4209-2

Batch or Lot Expiration Information

Lot# Lots: NR-071118A Exp. 07/20; NR-071218A Exp. 07/20; NR-071218C Exp. 07/20; NR-081017M Exp. 08/19; NR-110117H Exp. 11/19; NR-020118K Exp. 02/20; NR-111517C Exp. 11/19; NR-120317J Exp. 12/19

Recall Number: D-0765-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
537 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Yeast Freee..., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955007623, NDC 57955-0102-2

Batch or Lot Expiration Information

Lot# Lots: 081116A Exp. 08/19; 022417B Exp. 02/20

Recall Number: D-0636-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
1980 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Ear Ringing, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955527527, NDC 57955-5275-2

Batch or Lot Expiration Information

Lot# Lots: 052516V Exp. 05/19; 052517E Exp. 05/20

Recall Number: D-0876-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
44 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Birth Ease, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000228, NDC 57955-0002-2

Batch or Lot Expiration Information

Lot# Lot: 090116E Exp. 09/19

Recall Number: D-0728-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
59 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx ScarCure, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955008729, NDC 57955-0087-2

Batch or Lot Expiration Information

Lot# Lot: 012317A Exp. 01/20

Recall Number: D-0717-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
54 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Allergies: Shellfish & Seafood Allergy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955220121, NDC 57955-2201-2

Batch or Lot Expiration Information

Lot# Lots: 080315H Exp. 08/18; 010918H Exp. 01/20

Recall Number: D-0730-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
21 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Aversion to Exertion Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955279020, NDC 57955-2790-2

Batch or Lot Expiration Information

Lot# Lots: 063015F Exp. 06/18; 012517F Exp. 01/20

Recall Number: D-0891-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
24 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Overly-Sensitive, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955207023, NDC 57955-2071-2

Batch or Lot Expiration Information

Lot# Lot: 112117H Exp. 11/19

Recall Number: D-0742-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
260 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx TMJ/Jaw Formula Oral Health, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955003229, NDC 57955-0032-2

Batch or Lot Expiration Information

Lot# Lots: 072815H Exp. 07/18; 020917C Exp. 02/20

Recall Number: D-0555-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
26410 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Lungs & Bronchial Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955505327, NDC 57955-5053-2

Batch or Lot Expiration Information

Lot# Lot Numbers: 021718D Exp. 02/20; 091415H Exp. 09/18; 012616G Exp. 01/19; 033116A Exp. 03/19; 072916D Exp. 07/19; 091616A Exp. 0919; 121916C Exp. 12/19; 052517F Exp. 05/20; 112317C Exp. 11/19

Recall Number: D-0943-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
17395 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #1 Earth Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4201-2

Batch or Lot Expiration Information

Lot# Lots: NR-031516N Exp. 03/19; NR-073015C Exp. 07/18; NR-010617A Exp. 01/20; NR-011216L Exp. 01/19; NR-021717A Exp. 02/20; NR-050916E Exp. 05/19; NR-060517A Exp. 06/20; NR-061616A Exp. 06/19; NR-080116D Exp. 08/19; NR-090115C Exp. 09/18; NR-090616A Exp. 09/19; NR-101416A Exp. 10/19; NR-120815A Exp. 12/18; NR-020118A Exp. 02/20; NR-022318A Exp. 02/20; NR-051618B Exp. 05/20; NR-071718E Exp. 07/20; NR-110817A Exp. 11/19; NR-103117A Exp. 10/19; NR-120317A Exp. 12/19

Recall Number: D-0634-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
90 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic UlcerPlex Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955507420, NDC 57955-5074-2

Batch or Lot Expiration Information

Lot# Lots: 051716D Exp. 05/19; 100316H Exp. 10/19

Recall Number: D-0764-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
17 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Aller-Detox: Water Chemicals U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955340027, NDC 57955-3400-2

Batch or Lot Expiration Information

Lot# Lot: 022516A Exp. 02/19

Recall Number: D-0873-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
290 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Acne Clear, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955004127, NDC 57955-0041-2

Batch or Lot Expiration Information

Lot# Lots: 091616K Exp. 09/19; 081617A Exp. 08/19

Recall Number: D-0810-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
296 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Leg Cramps & Spasms, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955043522, NDC 57955-0435-2

Batch or Lot Expiration Information

Lot# Lots: 072015J Exp. 07/18; 051716H Exp. 05/19; 081016B Exp. 08/19; 092617B Exp. 10/19

Recall Number: D-0857-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
205 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Diarrhea Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955002024, NDC 57955-0020-2

Batch or Lot Expiration Information

Lot# Lots: 072815N Exp. 07/18; 081816A Exp. 08/19

Recall Number: D-0902-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
6153 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Aquaflora Phase I Candida Control Program, Net 16 fl. oz. (1 PT) 473 mL, Homeopathic Formula, Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955160168, NDC 57955-1601-6

Batch or Lot Expiration Information

Lot# Lots: 022218D Exp. 02/20; 100917D Exp. 10/19; 021717A Exp. 02/20; 041816B Exp. 04/19; 062816F Exp. 06/19; 122815B Exp. 12/18

Recall Number: D-0883-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
95 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Procrastination, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955276029, NDC 57955-2761-2

Batch or Lot Expiration Information

Lot# Lots: 091715C Exp. 09/18; 091316C Exp. 09/19

Recall Number: D-0785-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
552 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's SafeCare Rx Fear & Phobia, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955179023,NDC 57955-1791-2

Batch or Lot Expiration Information

Lot# Lots: 072015E Exp. 07/18; 032216G Exp. 03/19; 102816E Exp. 10/19

Recall Number: D-0621-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
172 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
Dr. King's Natural Medicine Homeopathic Climate Adaptation Hot & Humid, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955528524, NDC 57955-0173-2

Batch or Lot Expiration Information

Lot# Lots: 022916C Exp. 02/19; 062415Y Exp. 06/18; 071316B Exp. 07/19

Recall Number: D-0937-2019

Reason for Recall
Microbial contamination
Initiated
07-20-2018
Reported
03-20-2019
Quantity
595 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80601
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
King Bio Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide, Canada, and Australia.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
01-19-2022
Product Description About Product Description
Full technical description of the product.
NET Remedies #6 (Orange Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Batch or Lot Expiration Information

Lot# Lots: AUS-020118C Exp. 02/20; AUS-022418C Exp. 02/20; AUS-071718T Exp. 07/20; AUS-101117C Exp. 10/19