Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Phar...
FDA Recall #D-0195-2025 — Class III — December 12, 2024
Product Description
Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.
Reason for Recall
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recalling Firm
Akron Pharma, Inc. — Fairfield, NJ
Classification
Class III — Not likely to cause adverse health consequences.
Product Type
Drugs
Product Quantity
14825 bottles
Distribution
Nationwide in the US
Code Information
Lot #s: KDT0124004, KDT0124005, KDT0124006, Exp 08/31/2026
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated