Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W B...
FDA Recall #D-0193-2025 — Class III — December 12, 2024
Product Description
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 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
768 bottles
Distribution
Nationwide in the US
Code Information
Lot: KDT0224002A, Exp 09/30/2026
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated