Multi-event January 2017 FDA Recall Drug by Cherry Hill Sales Co.

This Multi-event Class II drug recall was voluntarily initiated by Cherry Hill Sales Co. on January 27, 2017 for the product Drug. The FDA reported the reason for recall as cgmp deviations. The product was distributed in Michigan, Illinois, New York, Florida, Pennsylvania . and the recall is currently terminated.

Reported Recall Events

D-0483-2017 TERMINATED D-0487-2017 TERMINATED D-0484-2017 TERMINATED D-0485-2017 TERMINATED D-0486-2017 TERMINATED

Recall Number: D-0483-2017

Reason for Recall
CGMP Deviations
Initiated
01-27-2017
Reported
03-01-2017
Quantity
3,600 cartons

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
76407
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.
Cherry Hill Sales Co.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Michigan, Illinois, New York, Florida, Pennsylvania .
Termination Date About Termination Date
Date that FDA officially terminated the recall.
04-19-2017
Product Description About Product Description
Full technical description of the product.
MakeSense PHARMA, HEMORRHOIDAL RELIEF CREAM Phenylephrine HCL-0.25% Zinc Oxide-12.50%,1 oz. (28 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-205-28

Batch or Lot Expiration Information

Lot# 103811; Exp. 09/17
Lot# 105304; Exp. 04/18 NDC 69020-205-28 UPC 857181005108

Recall Number: D-0487-2017

Reason for Recall
CGMP Deviations
Initiated
01-27-2017
Reported
03-01-2017
Quantity
2,400 cartons

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
76407
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.
Cherry Hill Sales Co.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Michigan, Illinois, New York, Florida, Pennsylvania .
Termination Date About Termination Date
Date that FDA officially terminated the recall.
04-19-2017
Product Description About Product Description
Full technical description of the product.
MakeSense PHARMA ANTIFUNGAL CREAM Clotrimazole 1%, 1.25 oz. (35 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-203-35

Batch or Lot Expiration Information

Lot# 103803; Exp. 08/17 NDC 69020-203-35 UPC 857181005023

Recall Number: D-0484-2017

Reason for Recall
CGMP Deviations
Initiated
01-27-2017
Reported
03-01-2017
Quantity
7,200 cartons

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
76407
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.
Cherry Hill Sales Co.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Michigan, Illinois, New York, Florida, Pennsylvania .
Termination Date About Termination Date
Date that FDA officially terminated the recall.
04-19-2017
Product Description About Product Description
Full technical description of the product.
MakeSense PHARMA FIRST AID CREAM Lidocaine HCL 0.5%, Phenol 0.5%, 1 oz.. (28 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-210-28

Batch or Lot Expiration Information

Lot# 103814; Exp. 09/17
Lot# 105306; Exp. 04/18 NDC 69020-210-28 UPC 85718005139

Recall Number: D-0485-2017

Reason for Recall
CGMP Deviations
Initiated
01-27-2017
Reported
03-01-2017
Quantity
4,800 cartons

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
76407
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.
Cherry Hill Sales Co.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Michigan, Illinois, New York, Florida, Pennsylvania .
Termination Date About Termination Date
Date that FDA officially terminated the recall.
04-19-2017
Product Description About Product Description
Full technical description of the product.
MakeSense PHARMA Medicated ANTI-ITCH CREAM WITH SOOTHING ALOE VERA AND VITAMIN E, Camphor-1% Menthol-1%, 1oz.(28 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-201-28

Batch or Lot Expiration Information

Lot# Lot: 103814; Exp. 08/17 NDC 69020-201-28 UPC 85718005016

Recall Number: D-0486-2017

Reason for Recall
CGMP Deviations
Initiated
01-27-2017
Reported
03-01-2017
Quantity
2,400 cartons

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
76407
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.
Cherry Hill Sales Co.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Michigan, Illinois, New York, Florida, Pennsylvania .
Termination Date About Termination Date
Date that FDA officially terminated the recall.
04-19-2017
Product Description About Product Description
Full technical description of the product.
MakeSense PHARMA ANTIFUNGAL CREAM 1 oz. Miconazole Nitrate 2%, 1 oz. (28 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-208-28

Batch or Lot Expiration Information

Lot# 103810; Exp. 09/17
Lot# 105303; Exp. 04/18 NDC 69020-208-28 UPC 857181005092