Presence of particulate matter: Visible glass flakes identified as lamellae in some drug product vials.
Presence of particulate matter: Visible glass flakes identified as lamellae in some drug product vials.
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 Amgen, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1086-2017 — Amgen, Inc. Amgen, Inc. recalls Procrit Epoetin Alfa 40,000 units/mL single use vial For Intravenou Hello, I own a Amgen, Inc. recalls Procrit Epoetin Alfa 40,000 units/mL single use vial For Intravenouse or Subcutaneous Use Only, Rx only, Manufactured that is covered by recall D-1086-2017 from Amgen, 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.
