Recall D-1352-2022
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
Recall D-1352-2022 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | D-1352-2022 |
| Event ID | 90682 |
| Distribution | Product was distributed to 6 distributors/wholesalers who may have further distributed the product. |
| Quantity | 301,382 bottles |
| Recall Reason | Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet. |
| Drug Classification | Class III |
| Drug Code Info | 20220824 |
| Recall Initiation Date | 20220804 |
| Report Date | 20220824 |
| Classification Date | 20220817 |
| Address | 373 Us Highway 46 Ste 117 Fairfield, NJ 07004-2456 United States |
| Recalling Firm | Akron Pharma, Inc. |
| Initial Notification | Letter |
| Similar To |