Aripiprazole Recall: Generic 10 mg Rx tablets
Announced 2026-07-29 · FDA
FDA recall for Aripiprazole Tablets, USP, 10 mg, 30-count Rx bottles. The recall involves Lot 24144162, expiration 09/2027, affecting 2,256 bottles distributed nationwide. The product was manufactured by Alken Laboratories Ltd. in India and distributed in the United States by Ascend Laboratories, LLC, Parsippany, NJ.
| Brand | Ascend Laboratories, LLC |
|---|---|
| Product | Aripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx only, Manufactured by: Alken Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. NDC: 67877-432-03 |
| Reason | Superpotent drug |
| Severity | moderate |
| Units affected | 1753 |
| Distribution | Nationwide in the USA. |
| Agency | FDA |
| Recall / campaign no. | Lot #: 24144162, Exp. Date 09/2027 |
WHAT YOU SHOULD DO
- Check your bottles for Lot 24144162 and the expiration date 09/2027; do not use any affected bottles.
- Contact Ascend Laboratories, LLC or your healthcare provider for instructions on return, disposal, or replacement.
- If you have used this product and have concerns or experience symptoms, seek medical advice promptly and report any adverse effects.
Other Ascend Laboratories, LLC recalls
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.