B Braun Medical recalls specific IV administration sets used with pumps that may cause medication backflow or inability to prime, leading to potential errors in treatment.
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 administration sets used with gravity and pump systems. These sets could allow medication to flow backward into the main IV line or become blocked, which might cause treatment errors.
The IV sets may allow medication from a secondary container to flow back into the primary IV line. They can also become blocked (occluded), making it impossible to properly prime the set and potentially causing treatment errors.
Healthcare professionals using these IV sets with pumps like Infusomat Space, Outlook, or Vista Basic are most at risk. Patients receiving IV treatments with the recalled sets could face medication errors.
Check for catalog numbers 490241, 490298, or 490360 on the IV sets. These sets were sold with specific pump models including Infusomat Space, Outlook, and Vista Basic.
Look for the catalog number on the IV set: 490241, 490298, or 490360.
Reach out to B Braun Medical for guidance on whether your set is affected and next steps.
The recall affects IV sets used with Infusomat Space, Outlook, and Vista Basic pumps.
Check for catalog numbers 490241, 490298, or 490360 on the IV set.
The recall does not require immediate stop use; contact B Braun Medical for specific guidance.
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-0652-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0652-2026 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.
