Recall
FDAHealthMay 28, 2026

Ajanta Pharma USA Inc — Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules, Manufactured by: Ajanta Pharma Limited, India, Marketed by: Ajanta Pharma USA Inc. Bridgewater, NJ 08807, NDC 27241-120

⚠️ CGMP Deviations

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
May 28, 2026

U.S. Nationwide

What's affected?

Product
Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules, Manufactured by: Ajanta Pharma Limited, India, Marketed by: Ajanta Pharma USA Inc. Bridgewater, NJ 08807, NDC 27241-120-04.
UPC
0327241119040
Lot code
PA02216

Additional details

Lot # PA02216; Exp. 12/2029

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 3648 bottles.

View original FDA notice →

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