Someone else had posted this recall a few days ago. I received an alert from the Natl. Pain Foundation on this recall. From what I have read these are the generic patches. For what ever reason Actavis did not see fit to notify the general public of this recall and the FDA is is stepping in on this. The recall is because the patches are releasing too much medication. Actavis stated this does not pose a serious threat of injury or death. What rock did they crawl out from under I wonder. By releasing too much medication it can cause increased sedation, nausea and vomitting and slowed breathing.
The FDA says to contact Actavis and demand a consumer recall and proper replacement. The Return/Reimbursement phone number is 1-888-896-4562.
Also contact the FDA and report any adverse reactions to fda.gov/medwatch/report.htm
The FDA recommends the following if you are possession of these patches;
Notify the dr that rx'd the patches to you.
Request a new script.
Contact the pharmacy that dispensed the patches and let them know of the recall.
Notify your insurance of the recall so you will not have a problem getting replacement patches paid for.
Moderator Chronic Pain Forum