Class III Recall

Akron Pharma, Inc.

Product
Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01.
Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Classification
Class III
Status
Ongoing
Lot
Lot: KDT0224002A, Exp 09/30/2026
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