Akron Pharma, Inc.: Drug Recall
Recall #D-0195-2025 · 12/12/2024
Class III: Low Risk
Recall Details
- Recall Number
- D-0195-2025
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- Akron Pharma, Inc.
- Status
- Ongoing
- Date Initiated
- 12/12/2024
- Location
- Fairfield, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 14825 bottles
Reason for Recall
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Product Description
Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.
Distribution Pattern
Nationwide in the US
Other Recalls by Akron Pharma, Inc.
- Class III: Low Risk 12/12/2024
- Class III: Low Risk 12/12/2024
- Class III: Low Risk 12/12/2024
- Class III: Low Risk 12/12/2024
- Class III: Low Risk 12/12/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.