Ajanta Pharma USA Inc: Aripiprazole Tablets Usp
Recall Summary Ajanta Pharma USA Inc. is recalling bottles of Aripiprazole Tablets USP 30 mg (NDC 27241-056-03) distributed nationwide because some bottles were mislabeled and actually contain Voriconazole Tablets 50 mg instead. The affected product was made in India and marketed by Ajanta Pharma USA Inc. in Bridgewater, NJ. This mix-up affects patients who may have received the wrong medication without knowing it.
- Recalling firm
- Ajanta Pharma USA Inc
- Product
- Aripiprazole Tablets USP, Rx only, 30 mg, 30 tablets, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-056-03.
- Reason
- Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
- Classification
- Class II
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-05-27
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- U.S. Nationwide
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/0bbd32b2-4f40-44ae-be44-7e87f30a4b7e