Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Actavis to request your refund or repair — edit it as you like.
Subject: Recall D-599-2013 — Actavis Actavis recalls Fentanyl Transdermal System, 50 mcg/h, 1 system per pouch (NDC 0591-3212-54) Hello, I own a Actavis recalls Fentanyl Transdermal System, 50 mcg/h, 1 system per pouch (NDC 0591-3212-54), packaged in 5-count systems per box (NDC that is covered by recall D-599-2013 from Actavis. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
