MedicineWatch US
Class III Recall

Akron Pharma, Inc.

Product
Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.
Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Classification
Class III
Status
Ongoing
Lot
Lot #s: KDT0124004, KDT0124005, KDT0124006, Exp 08/31/2026
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.
Akron Pharma, Inc. — Class III Recall | MedicineWatch US