Duragesic pain patches were recalled in February, 2008, due to a manufacturer’s defect which could result in Fentanyl overdose in users.

The Duragesic recall only included 25-microgram-per hour patches. It is estimated that roughly two of every million patches could be defective; however, due to the extreme potency of the active ingredient, Fentanyl, these chances should not be risked under any circumstances.

Duragesic 25-microgram-per-hour patches are manufactured by Johnson & Johnson and are sold by J&J’s PriCara unit, Sandoz, and Alza Corp. All defective Duragesic/Fentanyl pain patches have expiration dates on or before December 2009.

FDA Fentanyl Recall

On Feburary 12, 2008, the FDA released a statement warning patients and doctors against the use of Duragesic 25-microgram/hour patches. The FDA warned against the possible leakages which may be found in the patches, and provided information on how to get rid of defective patches.

Due to the strength of Fentanyl, even coming into contact with a small amount can result in serious side effects in patients. This realization spurred the voluntary recall of Duragesic patches.

For more information about the FDA Duragesic recall visit the FDA’s website or call our law office at (800) 732-3070 or use our online contact form.
 

Defective Fentanyl Pain Patch

Duragesic pain patches are gel filled patches which are applied to the user’s skin. The active ingredient in Duragesic patches is Fentanyl – found as the gel like substance in the patch.

In the defective Duragesic 25-microgram-per-hour patches there is a slit along one side of the patch allowing the Fentanyl to leak out. Fentanyl is a potent opiate which is 80 times stronger than morphine. Over absorption of Duragesic/Fentanyl results in serious side effects and death.

Unfortunately, Duragesic 25-microgram-per-hour patches are commonly prescribed to lower weight patients and children – who may not be able to express their side effects and symptoms. Children should especially be monitored while using Duragesic pain patches.
 

Previous Duragesic Recall

The 2008 Duragesic pain patch recall was not the first recall issued by Johnson & Johnson. In 2004 Duragesic pain patches were also recalled due to another leakage issue.

The 2004 Duragesic recall included all dosages of the pain patch and resulted in hundreds of deaths across the United States.
 

Fentanyl Death Attorney

If you or a loved one has been a victim of recalled Duragesic patches contact McEwen Law Firm today. Our attorneys have extensive knowledge about the Duragesic/Fentanyl recall and are dedicated to providing you with the compensation you deserve.

McEwen Law Firm offers free no obligation consultations and we work on a contingency, meaning you don’t pay a dime unless we win your case. For more information or to contact an attorney today please call (800) 732-3070 or fill out our contact form today.