Actavis recalls Fentanyl Transdermal System, 50 mcg/h, 1 system per pouch (NDC 0591-3212-54), packaged in 5-count systems per box (NDC 0
Recalled June 19, 2013 · FDA recall D-599-2013 · Actavis
Hazard
Failed Impurities/Degradation Specifications · FDA Class III
Units
98,952 boxes
Sold at
Nationwide
Description
Failed Impurities/Degradation Specifications
Product
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.
Manufacturer(s)
Actavis
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →