Family Dollar Stores, Llc.: Drug Recall

Recall #D-1373-2022 · 06/23/2022

Class II: Risk

Recall Details

Recall Number: D-1373-2022
Classification: Class II
Product Type: Drug
Recalling Firm: Family Dollar Stores, Llc.
Status: Ongoing
Date Initiated: 06/23/2022
Location: Chesapeake, VA, United States
Voluntary/Mandated: Voluntary: Firm initiated

Reason for Recall

CGMP Deviations: product held outside appropriate storage temperature conditions.

Product Description

MOTRIN IB CAPLETS 24CT SKU999394; GOOD SENSE IBUPROFEN 200MG TABLETS 24CT SKU 900556;GOOD SENSE IBUPROFEN 200MG CAPLET 50 CT SKU 902333 MOTRIN CHILDREN'S BUBBLEGUM 4 FL OZ SKU 903048 GOOD SENSE IBUPROFEN REGULAR SOFTGELS 160CT SKU 999373 GOOD SENSE IBUPROFEN 200 MG CAPLET 100 CT SKU 902359 MOTRIN IB CAPLET 50 CT SKU 900604 GOOD SENSE IBUPROFEN IB CAPLET 100 CT SKU 913989 GOOD SENSE IBUPROFEN 200 MG SOFTGEL 20CT SKU 916994 ADVIL LIQUID GEL 40 CT SKU 916071 GOOD SENSE IBUPROFEN PM 200 MG 20 CT SKU 917004 ADVIL PM CAPLET 20CT SKU 913010 GOOD SENSE IBUPROFEN TABLET 100 CT SKU 913991 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022. Specifically:

Distribution Pattern

Nationwide within the United States

Other Recalls by Family Dollar Stores, Llc.

Class II: Risk 03/31/2023

CGMP deviation: product outside labeled storage temperature requirements.
Class II: Risk 03/31/2023

CGMP deviation: product outside labeled storage temperature requirements.
Class II: Risk 03/31/2023

CGMP deviation: product outside labeled storage temperature requirements.
Class II: Risk 03/31/2023

CGMP deviation: product outside labeled storage temperature requirements.
Class II: Risk 08/10/2022

cGMP deviation: Product held outside of appropriate temperature storage conditions.

View all recalls by Family Dollar Stores, Llc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.