Subpotent Drug: OOS (out of specification) assay result at the 12 month stability time point.
Subpotent Drug: OOS (out of specification) assay result at the 12 month stability time point.
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 Actelion Pharmaceuticals U.S., Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-143-2013 — Actelion Pharmaceuticals U.S., Inc. Actelion Pharmaceuticals U.S., Inc. recalls Ventavis (iloprost) Hello, I own a Actelion Pharmaceuticals U.S., Inc. recalls Ventavis (iloprost) Inhalation Solution, 10 mcg/1 mL, Sterile, 30 Single Use Ampules per carton, Manufactured for that is covered by recall D-143-2013 from Actelion Pharmaceuticals U.S., Inc.. 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.
