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NOTE: As of February 12, 2008 the FDA.announced a PARTIAL Duragesic Patch Recall. Duragesic Press Release from PriCara, Division of Ortho-McNeil-Janssen Pharmaceuticals, Inc PriCara RECALLS 25 mcg/hr DURAGESIC® (fentanyl transdermal system) CII PAIN PATCHES NOTE: Other Strength Patches (12.5, 50, 75 and 100 mcg/hr) NOT Affected. All patients that are using affected Duragesic patches or others affected by the recall of Duragesic Patches, should contact their doctors immediately to discuss other medical options that may be available to them. This site is not intended to provide medical information and should not be relied on by anyone. All patients with questions concerning the Duragesic Patch Recall or medical problems should immediately speak to their doctors. This website is not affliated with the manufacturers of Duragesic,any distrubutor. All trademarks are owned by the owners of such trademarks
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