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Home » J&J Recalls Two Pain Patch Lots, Identifies Root Cause
J&J Recalls Two Pain Patch Lots, Identifies Root Cause
January 13, 2009
Two lots of Johnson & Johnson’s (J&J) fentanyl transdermal patches were recalled last month because the products might have a cut along the one side of the drug reservoir, which would cause them to leak and could expose patients to dangerously high amounts of the narcotic.