B Braun recalls specific anesthesia IV sets used with pumps due to potential medication backflow and inability to prime, risking contamination and occlusion.
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 anesthesia IV sets used with gravity or pump administration systems because they can cause medication to flow backward into the main IV line and fail to prime properly. This could lead to contamination or blockages in the IV system.
The IV sets can allow medication from secondary containers to flow back into the primary IV line, potentially contaminating the main medication. They may also fail to prime correctly, causing blockages (occlusion) in the IV system.
Healthcare professionals using the recalled IV sets with B Braun pumps are most at risk. Patients receiving IV treatments with these sets could be affected if the sets are not properly maintained.
Check for the catalog numbers 490469 or 490470 on the IV sets. These sets were sold with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Look for catalog numbers 490469 or 490470 on the IV set to confirm if it is recalled.
The sets can cause medication to flow backward into the primary IV line and fail to prime properly, leading to contamination or blockages.
The recalled sets are used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Check for catalog numbers 490469 or 490470 on the IV set label.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0607-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0607-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.