Lack of Assurance of Sterility: Glass vials may have finish fractures and glass particles.
Lack of Assurance of Sterility: Glass vials may have finish fractures and glass particles.
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 Fresenius Kabi USA, LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0296-2015 — Fresenius Kabi USA, LLC Fresenius Kabi USA, LLC recalls ONDANSETRON INJECTION, USP, 4 mg/ 2 mL (2 m Hello, I own a Fresenius Kabi USA, LLC recalls ONDANSETRON INJECTION, USP, 4 mg/ 2 mL (2 mg/mL), For IM or IV Use, Single Dose 2 mL Vials, Rx only. APP that is covered by recall D-0296-2015 from Fresenius Kabi USA, LLC. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
