B Braun Medical recalls extension sets for IV pumps that may cause medication backflow into primary IV containers. Affected units have specific catalog numbers and are used with Infusomat pumps. Stop using immediately to prevent potential medication contamination.
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 because they can cause medication to flow backward into the main IV container and fail to prime properly. This could lead to medication contamination or incorrect dosing if the set is not used correctly.
The extension sets can allow medication from secondary IV containers to flow back into the primary container. They may also become blocked (occluded), preventing the proper priming of the IV system and causing medication delivery issues.
Healthcare professionals using IV pumps with B Braun extension sets are most at risk. Patients receiving IV treatments with these specific sets may also be affected.
Check for the catalog number 490202 on the extension set. These sets are used with B Braun Infusomat pumps including Space, Outlook, and Vista Basic models. They were sold with specific UDI-DI numbers.
Discontinue use of the extension set with B Braun Infusomat pumps to prevent medication backflow and occlusion.
The catalog number is 490202.
These sets are used with Space, Outlook, and Vista Basic pumps.
Look for the catalog number 490202 on the extension set or check the UDI-DI numbers provided in the recall notice.
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-0632-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0632-2026 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.
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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.
