Recall
FDAHealthMay 27, 2026

Ajanta Pharma USA Inc — 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.

⚠️ Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
May 27, 2026

U.S. Nationwide

What's affected?

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.
UPC
0327241051036
Lot code
PA00805

Additional details

Lot: PA00805, expires: 01/31/2029

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 6,143 bottles.

View original FDA notice →

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