WhichRecall
Class I — UrgentReported 2025-02-26

Fentanyl Transdermal System CII, 25mcg/h, packaged in a pouch, further packaged in 5-count carton, Rx only, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058, Manufactured by: Kindeva Drug Delivery L/P, Northridge, CA 91324, NDC 47781-424-47.

Recalled by Alvogen, Inc

Reason for Recall

Defective delivery system - patches could be multi-stacked, adhered one on top of the other, in a single product pouch.

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Recall Number
D-0245-2025
Classification
Class I
Status
Ongoing
Category
drug
Initiated
2025-01-31
Reported
2025-02-26
Distribution
USA Nationwide
Code Info
Lot #: 108319, Exp: 04/30/2027
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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