Drug recall D-0594-2026
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 for recall
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
Lots and codes
Lot: PA00805, expires: 01/31/2029
Recall details
- Recalling firm
- Ajanta Pharma USA Inc, Bridgewater, NJ
- Quantity
- 6,143 bottles
- Distribution
- U.S. Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- May 27, 2026
Related products
- Aripiprazole – drug information
- NDC 27241-055 Aripiprazole · Aripiprazole 20 mg/1 · Ajanta Pharma USA Inc.
- NDC 27241-056 Aripiprazole · Aripiprazole 30 mg/1 · Ajanta Pharma USA Inc.
- NDC 27241-054 Aripiprazole · Aripiprazole 15 mg/1 · Ajanta Pharma USA Inc.
- NDC 27241-051 Aripiprazole · Aripiprazole 2 mg/1 · Ajanta Pharma USA Inc.
- NDC 27241-053 Aripiprazole · Aripiprazole 10 mg/1 · Ajanta Pharma USA Inc.
- NDC 27241-052 Aripiprazole · Aripiprazole 5 mg/1 · Ajanta Pharma USA Inc.