D-0195-2025 Class III Ongoing
FDA drug recall D-0195-2025 was initiated by Akron Pharma, Inc. on December 12, 2024 and is designated Class III. Reason for recall: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID. The recall status is ongoing. Affected quantity: 14825 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- January 22, 2025
- Initiation Date
- December 12, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 14825 bottles
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.
Distribution Pattern
Nationwide in the US
Code Information
Lot #s: KDT0124004, KDT0124005, KDT0124006, Exp 08/31/2026