Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 ...

FDA Recall #D-0194-2025 — Class III — December 12, 2024

Recall #D-0194-2025 Date: December 12, 2024 Classification: Class III Status: Ongoing

Product Description

Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8024-01 .

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

6429 bottles

Distribution

Nationwide in the US

Code Information

Lot #: KDT0124001, Exp 08/31/2026

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated