NEWS: February 13, 2008

Johnson & Johnson Duragesic Pain Patch Flaw Recall

A recall has been issued by Johnson & Johnson and Novartis AG’s Sandoz on 25-microgram-per-hour patches with expiration dates on or before December 2009.

It was found that a manufacturing problem led to some of the patches having a cut in the internal reservoir lining. This cut may cause a leaking problem of the patch.

The danger is if anyone touches a defective pain patch they may be delivered a dose of the prescription painkiller fentanyl which may lead to breathing problems or even an accidental overdose.

Back in December the FDA issued a safety warning on the Duragesic patch, citing improper use may cause breathing difficulties and death.

The FDA continues to work with J& J on this voluntary recall and is investigating this latest issue.

For more information on the Duragesic Pain Patch Recall please visit: http://www.resource4duragesicrecall.com/