Multi-event July 2019 FDA Recall Drug by Herbal Doctor Remedies

This Multi-event Class II drug recall was voluntarily initiated by Herbal Doctor Remedies on July 12, 2019 for the product Drug. The FDA reported the reason for recall as cgmp deviations. The product was distributed Nationwide and the recall is currently terminated.

Reported Recall Events

D-1629-2019 TERMINATED D-1602-2019 TERMINATED D-1606-2019 TERMINATED D-1608-2019 TERMINATED D-1594-2019 TERMINATED D-1597-2019 TERMINATED D-1593-2019 TERMINATED D-1610-2019 TERMINATED D-1626-2019 TERMINATED D-1598-2019 TERMINATED D-1622-2019 TERMINATED D-1616-2019 TERMINATED D-1590-2019 TERMINATED D-1627-2019 TERMINATED D-1600-2019 TERMINATED D-1609-2019 TERMINATED D-1623-2019 TERMINATED D-1587-2019 TERMINATED D-1625-2019 TERMINATED D-1607-2019 TERMINATED D-1617-2019 TERMINATED D-1596-2019 TERMINATED D-1592-2019 TERMINATED D-1591-2019 TERMINATED D-1618-2019 TERMINATED D-1611-2019 TERMINATED D-1603-2019 TERMINATED D-1624-2019 TERMINATED D-1620-2019 TERMINATED D-1605-2019 TERMINATED D-1628-2019 TERMINATED D-1604-2019 TERMINATED D-1599-2019 TERMINATED D-1588-2019 TERMINATED D-1621-2019 TERMINATED D-1619-2019 TERMINATED D-1615-2019 TERMINATED D-1613-2019 TERMINATED D-1595-2019 TERMINATED D-1589-2019 TERMINATED D-1614-2019 TERMINATED D-1601-2019 TERMINATED D-1612-2019 TERMINATED

Recall Number: D-1629-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Fungo Off Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1602-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Herpes-S, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1606-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Lump Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1608-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Lung Saver Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1594-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Dragon Pain Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1597-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Fungo Balm, 30 gram, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1593-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Deafness Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1610-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Migraine Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1626-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Appetrol Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1598-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Glauco-Catar Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1622-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Detensin, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1616-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Stomach Flu Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1590-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Baby Saver Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1627-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Anemia Off, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1600-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Herpes-G Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1609-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Lung Tonic EX Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1623-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Smoke End Capsules,Distributed Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1587-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Asma Aid Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1625-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Mental Tonic Capsules, Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1607-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Lung Fixer Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1617-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Stone Purger Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1596-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Edema Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1592-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Cardia Forte, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1591-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Bone Fixer, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1618-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Thyro-H, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1611-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Pain Away, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1603-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Herpes-V Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1624-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Thyro-Lo, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1620-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Worm Off, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1605-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Lube Lax Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1628-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Asma Stopper Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1604-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Lipidtrol Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1599-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Hair Back, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1588-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Asthma Balm 60 gram, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1621-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Yeast Douche Powder, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1619-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Vertigo Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1615-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Sperm Booster, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1613-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Prostatin Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1595-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Dragon Pain Oil, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1589-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Awake, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1614-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Psoriasis Balm, 60 gram, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1601-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Herpes-P, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry

Recall Number: D-1612-2019

Reason for Recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Initiated
07-12-2019
Reported
08-14-2019
Quantity
N/A

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
83437
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Herbal Doctor Remedies
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
N/A
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States and Brazil and on the internet
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-13-2023
Product Description About Product Description
Full technical description of the product.
Pain Stopper, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Batch or Lot Expiration Information

Lot# All lots within expiry