B Braun recalls certain IV extension sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected sets 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. EXTENSION SET W/ ULTRAPORT, 48 IN. (catalog number 490291). This recall is due to a risk of medication backflow from secondary IV containers into primary containers and the inability to properly prime the set, which could lead to incorrect medication administration.
The extension set can allow medication from a secondary IV container to flow back into the primary container. This can cause incorrect medication administration if the set is not properly primed, potentially leading to adverse effects.
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 set is not properly primed or if medication backflows.
Check for the extension set labeled 'EXTENSION SET W/ ULTRAPORT, 48 IN.' with catalog number 490291. These sets were sold with B Braun Infusomat pumps including Space, Outlook, and Vista Basic models.
Look for the label 'EXTENSION SET W/ ULTRAPORT, 48 IN.' with catalog number 490291 on the extension set.
Contact B Braun Medical Inc for further assistance if you have the recalled extension set.
The recalled extension set is labeled 'EXTENSION SET W/ ULTRAPORT, 48 IN.' with catalog number 490291.
The recalled extension set was sold with B Braun Infusomat Space, Outlook, and Vista Basic pumps.
Check for the label 'EXTENSION SET W/ ULTRAPORT, 48 IN.' with catalog number 490291 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-0634-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0634-2026 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.
