Akron Pharma, Inc.: Drug Recall
Recall #D-1352-2022 · 08/04/2022
Class III: Low Risk
Recall Details
- Recall Number
- D-1352-2022
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- Akron Pharma, Inc.
- Status
- Terminated
- Date Initiated
- 08/04/2022
- Location
- Fairfield, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 301,382 bottles
Reason for Recall
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Product Description
Acetaminophen 325 mg tablets, packaged in a) 100-count bottle (NDC 71399-8024-01); b) 1000-count bottle (NDC 71399-8024-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ
Distribution Pattern
Product was distributed to 6 distributors/wholesalers who may have further distributed the product.
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.