Medique Products: Drug Recall

Recall #D-0389-2022 · 12/06/2021

Class II: Risk

Recall Details

Recall Number
D-0389-2022
Classification
Class II
Product Type
Drug
Recalling Firm
Medique Products
Status
Terminated
Date Initiated
12/06/2021
Location
Fort Myers, FL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
3,260,400 tablets

Reason for Recall

CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.

Product Description

Physicians CARE Extra Strength PAIN RELIEVER [Acetaminophen, Aspirin (NSAID), and Caffeine], 250 mg, 250 mg, 65 mg, packaged as 100-count Tablets (50 Packets, 2 tablets each) per carton, Manufactured for: Acme United Corporation 55 Walls Dr, Fairfield, CT 06824, UPC 0 73577 90316 6

Distribution Pattern

Nationwide in the USA

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.