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Alvogen, INC

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Class I

  • The FDA’s most serious category — a reasonable probability of serious harm or death.
  • Refunds don't require a receipt, and you don't need proof of purchase.
  • FDA status: Ongoing.

What was recalled

Source: FDA · synced 29 Jul 2026 13:14
Check with your pharmacist Filed 2025-02-26

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

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.

Check these codes: Lot #: 108319, Exp: 04/30/2027

112,128 cartons (5 pouches/carton) · distributed usa nationwide Recall D-0245-2025 on FDA.gov ↗
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