Family Dollar Stores, Llc.: Drug Recall

Recall #D-1424-2022 · 06/23/2022

Class II: Risk

Recall Details

Recall Number: D-1424-2022
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
Product Quantity: Unknown

Reason for Recall

CGMP Deviations: product held outside appropriate storage temperature conditions.

Product Description

FW ASPIRIN CHEWABLE TABLET 36CT SKU 913990 GS ENTERIC ASPIRIN TABLET 120 CT SKU 913724 BAYER BACK BODY EX STRGTH CAPLETS 24CT SKU 900438 BAYER LOW DOSE 81 MG TABLET 120 CT SKU 916070 BAYER ASPIRIN 325MG TABLET 24CT SKU 913996 BAYER LOW DOSE TABLET 32CT SKU 915641 BAYER 81MG CHEWABLE TABLET 36 CT SKU 916078 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

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.