Fentanyl is a powerful opiate analgesic with potency approximately 81 times that of morphine. The Fentanyl Transdermal Patch (Duragesic) is used for chronic pain management. It has been classified by the U.S. authorities as a narcotic due to biological effects similar to those of heroin. Since Fentanyl's effects last for only a very short period of time, it is more addictive than heroin.

We take on Duragesic and Fentanyl claims and cases to get you the most possible compensation for your hardship and stress. Call our helpful professionals at (877) 701-0222 or contact us online.

Duragesic Recall

In 2004, the Johnson & Johnson subsidiaries that manufactured and marketed Duragesic recalled 5 lots of patches because of a "fold over defect" that could lead to leakage of the Fentanyl gel contained within the patches. Upon investigation by the FDA, numerous other defects were discovered and it became clear that there were leak defects in many other lots of all sizes that were not recalled.

In 2008, Johnson & Johnson (PriCara) recalled approximately 32 million patches because of possible leak defects. At the same time, distributor Actavis Inc. announced that 14 lots of its Fentanyl patches sold in the U.S. were being voluntarily recalled from wholesalers and pharmacies due to the "fold over defect" and widened the recall in March to include all remaining lots of its Transdermal patches.

Signs of Overdose

Signs of overdose include difficulty in breathing or shallow breathing, extreme sleepiness or sedation, an inability to walk or talk normally, dizziness, and feeling faint and confused. Patients who experience those symptoms should seek emergency medical attention as removing of the patch won't reverse the problem.

If you or someone you know has used the Duragesic Fentanyl Transdermal Patch or other Fentanyl products and has experienced any of its negative side effects, please contact our office immediately, at (877) 701-0222 or contact us online. You may have a case.