J&J, Novartis Recall Duragesic Pain Patches

Published on 23 October 2008 by admin in News

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Feb. 12 (Bloomberg) — Johnson & Johnson and Novartis AG’s Sandoz unit recalled some patches containing the painkiller fentanyl, saying manufacturing defects may cause leaks that can lead to fatal overdoses.

The Duragesic patches, made by Johnson & Johnson’s Alza Corp., may have a cut along the drug reservoir, exposing users directly to the fentanyl gel inside, the New Brunswick, New Jersey-based company said in a statement. It’s the fifth recall of some version of the patches since 1994.

“Perhaps the time has come for the FDA to order Johnson & Johnson to pull all versions of this product off the shelves,” said Alex MacDonald, a lawyer who represents the families of former patch users. Juries have found defective patches caused the deaths of two users since lawsuits over the products began going to trial in 2006.”

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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.

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