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drug_recall fentanylOn February 18, 2008, fourteen lots of the Actavis fentanyl patch, a prescription opioid pain medication, were voluntarily pulled off the shelves. Several weeks later, the recall was expanded to include all Actavis fentanyl patches sold in the United States.
The Actavis fentanyl patch was recalled because of serious fold-over defect risks, which can lead to accidental overdose. High doses of the pain medication can be delivered by direct contact if the Actavis fentanyl patch is defective, leading to serious respiratory distress and even death.
Have you suffered harm because of the Actavis Fentanyl patch?
If you or a loved one has suffered a serious adverse reaction caused by the Actavis fentanyl patch, such as overdose, respiratory problems, or even death, you may wish to contact a qualified attorney who can help you understand your legal rights and options. You may be able to obtain compensation for your losses and suffering through an Actavis fentanyl patch lawsuit. Please contact our qualified Actavis fentanyl attorneys today to learn more.
Which lots of the Actavis Fentanyl patch are affected by the recall?
The affected Actavis fentanyl patch products have expiration dates of May through August 2009. Different dosage levels of the affected Actavis fentanyl patch include 25, 50, 75, and 100 microgram per hour. The outside carton containing the Actavis fentanyl patch bears the name of the current maker, Actavis South Atlantic LLS, while some of the patch pouches bear the name of the company’s former name, Abrika Pharmaceuticals.
All of the recalled Actavis fentanyl patches have been distributed and sold exclusively in the United States. Actavis fentanyl patches sold in Europe are not affected by this recall.
What if I am in possession of the recalled Actavis fentanyl patch?
If you have any of the affected patches in your home, experts recommend that you dispose of them carefully. Being sure not to handle the Actavis fentanyl patch directly, you are urged to flush all unused patches down the toilet. If you happen to get any of the fentanyl gel on your person, rinse with lots of water (but no soap).
If you have questions about the Actavis fentanyl patch, you are encouraged to speak with your health care professional. Your doctor may be able to find you a safer alternative method of pain relief.
The Actavis fentanyl patch makers have issued the recall as a precautionary measure and have not received any official reports of injury related to the defective fentanyl patches. However, other reports of serious injury and death have been associated with fentanyl pain patches. In 2005, the FDA issued an advisory warning to communicate to patients the risks associated with the painkiller patches.
If you would like to learn more about the Actavis fentanyl patch, please contact us today.
Actavis Inc. has expanded its recent recall of fentanyl painkiller patches to include all lots sold in the United States. The company said the expansion is a precautionary measure because it cannot guarantee that all patches are without defect.
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