Presence of Particulate Matter: Product failed the appearance for the presence of visible particles under labeled storage condition.
Presence of Particulate Matter: Product failed the appearance for the presence of visible particles under labeled storage condition.
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 Alexion Pharmaceuticals, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1512-2014 — Alexion Pharmaceuticals, Inc. Alexion Pharmaceuticals, Inc. recalls Soliris (eculizumab), 300 mg/30 Hello, I own a Alexion Pharmaceuticals, Inc. recalls Soliris (eculizumab), 300 mg/30 mL (10 mg/mL), 30 mL Single-Use Vial, Rx only, Manufactured by: Alexion that is covered by recall D-1512-2014 from Alexion Pharmaceuticals, 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.
