FDA · Drugs · Wednesday, June 24

Aripiprazole Tablets USP, Rx only recall

Ajanta Pharma USA Inc recalled Aripiprazole Tablets USP, Rx only on June 24, 2026 because of product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg. It was sold nationwide.

Why it was recalled

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

What's recalled

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.

Quantity: 6,143 bottles

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company: Ajanta Pharma USA Inc, Bridgewater, NJ
Date: Wednesday, June 24
Severity: Class II
the product could cause temporary or reversible health problems.
Where sold: Nationwide
U.S. Nationwide
Status: Ongoing
Recall number: D-0594-2026
Source: U.S. Food and Drug Administration

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