B Braun Medical recalls extension sets for IV pumps that may cause medication backflow between IV containers, risking contamination. Affected units include specific catalog numbers and pump models.
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun Medical is recalling extension sets used with IV pumps to prevent medication from flowing backward into primary IV containers. This could lead to contamination or improper dosing if the set isn: t properly primed.
The extension sets may allow medication from secondary IV containers to flow back into primary containers. This can cause contamination or improper dosing if the set isn't properly primed, potentially leading to incorrect medication administration.
Healthcare professionals using IV pumps with the recalled extension sets are most at risk. Patients receiving IV treatments with these sets could face medication contamination.
Check for catalog number 490358 or primary UDI-DI 04046964642746 on the extension set. These sets were sold with BBMI's Infusomat Space, Outlook, and Vista Basic pumps.
Look for catalog number 490358 or primary UDI-DI 04046964642746 on the extension set.
The extension sets may allow medication to flow back from secondary IV containers into primary containers, causing contamination or improper dosing if not properly primed.
The affected pumps are BBMI's Infusomat Space, Outlook, and Vista Basic pumps.
Check for catalog number 490358 or primary UDI-DI 04046964642746 on the extension set.
We’ve drafted a message you can send B Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0633-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0633-2026 from B Braun Medical. 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.
