Lack of Assurance of Sterility
Lack of Assurance of Sterility
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 Infusion Options, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1810-2019 — Infusion Options, Inc. Infusion Options, Inc. recalls RITUXIMAB 575 MG / 250 ml 0.9% NACL IVPB; RIT Hello, I own a Infusion Options, Inc. recalls RITUXIMAB 575 MG / 250 ml 0.9% NACL IVPB; RITUXIMAB 675 MG / 250 ml 0.9% NACL IVPB; RITUXIMAB 1000 MG / 1000 ml NS that is covered by recall D-1810-2019 from Infusion Options, 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.
