B Braun recalls certain IV extension sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and are sold with certain pump models.
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun is recalling specific IV extension sets used with their Infus: 1. The extension sets could allow medication to flow backward from secondary IV containers into primary containers. 2. This could also prevent the sets from being properly primed, which is necessary for safe IV administration.
The extension sets may allow medication to flow backward from secondary IV containers into primary containers. This can cause medication to be improperly administered and could lead to the sets being unable to be primed properly, which is necessary for safe IV administration.
Healthcare professionals using B Braun Infusomat pumps with the recalled extension sets are most at risk. Patients receiving IV treatments with these sets could be affected if the extension sets are not properly primed.
Check for the catalog number 456520 or the UDI-DI 04046964296697 on the extension set. These sets were sold with B Braun Infusomat pumps including Space, Outlook, and Vista Basic models.
Look for the catalog number 456520 or UDI-DI 04046964296697 on the extension set.
The extension sets could allow medication to flow backward from secondary IV containers into primary containers and may not be able to be primed properly.
The affected extension sets were sold with B Braun Infusomat Space, Outlook, and Vista Basic pumps.
Check for the catalog number 456520 or UDI-DI 04046964296697 on the extension set.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0629-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0629-2026 from B Braun. 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.
