B Braun recalls gravity and pump IV sets used with Infusomat Space 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 certain IV administration sets used with Infus: 1) gravity IV sets and 2) pump sets with Infusomat Space pumps. The sets could allow medication to flow backward into the main IV line and cause blockages, which may lead to incorrect dosing or treatment complications.
The IV sets can allow medication from a secondary (piggyback) container to flow back into the primary IV container. This could cause incorrect dosing or blockages in the IV line, potentially leading to treatment complications.
Healthcare professionals using these IV sets with Infusomat Space pumps are most at risk. Patients receiving IV treatments with the recalled sets could experience medication errors or blockages.
Check for the catalog number 490349 on the IV set label. These sets are used with Infusomat Space pumps including Large Volume, Outlook, and Vista Basic models.
Look for the catalog number 490349 on the IV set label to confirm if it is affected.
The hazard is potential backflow of medication from secondary IV containers into primary containers and the inability to prime the IV line, which could cause incorrect dosing or blockages.
The affected pumps are Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump.
Check for the catalog number 490349 on the IV set label. These sets are used with Infusomat Space pumps.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0615-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0615-2026 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.
