Fentanyl Patch Recalled - FDA Release

Published on 23 October 2008 by admin in News

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FOR IMMEDIATE RELEASE — Morristown, NJ — February 17, 2008 — Actavis Inc., the United States manufacturing and marketing division of the international generic pharmaceutical company Actavis Group hf, today announced that 14 lots of Fentanyl transdermal system CII patches sold in the United States by Actavis’ subsidiary Actavis South Atlantic LLC are being voluntarily recalled from wholesalers and pharmacies as a precaution.

The recalled patches were manufactured by Corium International Inc., a contract manufacturer for Actavis, and sold nationwide in the United States by Actavis South Atlantic LLC.

Read Full Release At FDA Website

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