PlainRecalls
FDA Drug Low Class III Ongoing

Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.

Reported: January 22, 2025 Initiated: December 12, 2024 #D-0195-2025

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.

Details

Recalling Firm
Akron Pharma, Inc.
Units Affected
14825 bottles
Distribution
Nationwide in the US
Location
Fairfield, NJ

Frequently Asked Questions

What product was recalled?
Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.. Recalled by Akron Pharma, Inc.. Units affected: 14825 bottles.
Why was this product recalled?
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Which agency issued this recall?
This recall was issued by the FDA Drug on January 22, 2025. Severity: Low. Recall number: D-0195-2025.