WhichRecall
Class IIIReported 2026-03-11

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 capsules (4 individual packs containing 28 capsules each), NDC 69097-032-74; Inner carton: 28 capsules (4 blisters of 7 capsules), NDC 69097-032-56; Foil blister: NDC 69097-032-17

Recalled by Cipla USA, Inc.

Reason for Recall

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

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Recall Number
D-0382-2026
Classification
Class III
Status
Ongoing
Category
drug
Initiated
2026-02-18
Reported
2026-03-11
Distribution
U.S.A. Nationwide
Code Info
Lot #: 5GJ0223, Exp 04/30/2027
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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