FDAFDA · Food and drugs·Recall number D-599-2013
Fentanyl Transdermal System, 50 mcg/h, 1 system per pouch (NDC 0591-3212-54), packaged in 5-count systems per box (NDC 0591-3212-72), Rx only, Manufactured by Watson Laboratories, Inc, Corona, CA, 92880 USA; Distributed by: Watson Pharma, Inc.
Published June 19, 2013 · Recall initiated: June 3, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Actavis
- Distributor
- Nationwide
- Lot
- Lot #: Patch 453658; Carton 453658A, Exp 09/13
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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