B Braun Medical recalls IV extension sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and UDI-DI codes.
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 certain IV extension sets used with their Infusomat pumps because they can cause medication to flow backward into the main IV line and fail to prime properly. This could lead to incorrect dosing or infections if the backflow occurs.
The extension sets can allow medication from a secondary IV container to flow back into the primary IV line. This can also prevent the set from being properly primed, which may cause blockages or incorrect medication delivery.
Healthcare professionals using these extension sets with Infusomat pumps are most at risk. Patients receiving IV treatments with the recalled sets could face medication errors or infections.
Check for the catalog number V5405 or UDI-DI codes 04046964188978 and 04046964188961 on the extension set. These sets were sold with Infusomat pumps like the Space, Outlook, and Vista Basic models.
Look for the catalog number V5405 or UDI-DI codes 04046964188978 and 04046964188961 on the extension set.
The extension sets can cause medication to flow backward into the primary IV line and fail to prime properly, which may lead to incorrect dosing or infections.
The recalled extension sets were used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump.
Check for the catalog number V5405 or UDI-DI codes 04046964188978 and 04046964188961 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-0639-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0639-2026 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.
