Class III

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

Akron Pharma, Inc. · December 12, 2024

Reason for Recall

Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Distribution

Nationwide in the US

States Affected

NATIONWIDE

Quantity Affected

14825 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0195-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.