Ajanta Pharma USA Inc: Aripiprazole Tablets Usp
Aripiprazole Tablets 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. This mix-up affects patients who received this medication in all 50 states and Washington, D.C. Taking the wrong medication could cause serious health problems.
- 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/1d86ba2d-bbaa-41e5-87f5-593160a24a38