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Nilotinib Capsules, 200 mg per capsule, packaged in cartons, Rx only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, Outer carton: 112…

Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.

Class III Medicine & devices FDA March 11, 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
Cipla USA, Inc. — Warren, NJ
Severity
Class III — low
Reported
March 11, 2026
Quantity
164 cartons
Recall number
D-0382-2026
Status
Ongoing
Source
FDA

Where it went

U.S.A. Nationwide

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