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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.

CGMP Deviations

Class II Medicine & devices FDA July 1, 2026 Reached Texas
Read the official FDA notice →

What to do

Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.

Details

Recalling company
Ajanta Pharma USA Inc — Bridgewater, NJ
Severity
Class II — moderate
Reported
July 1, 2026
Quantity
3648 bottles
Recall number
D-0611-2026
Status
Ongoing
Source
FDA

Where it went

U.S. Nationwide

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