Medique Products: Drug Recall
Recall #D-0391-2022 · 12/06/2021
Class II: Risk
Recall Details
- Recall Number
- D-0391-2022
- 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
- 6,639,838 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
Extra Strength Headache (acetaminophen 250 mg, aspirin 250 mg, caffeine 65 mg) tablets, packaged in 2-count tablets per packet, Manufactured for: Lil' Drug Store Products, Inc., Cedar Rapids, IA 52404
Distribution Pattern
Nationwide in the USA
Other Recalls by Medique Products
- Class II: Risk 12/06/2021
- Class II: Risk 12/06/2021
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.