B Braun recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units include specific models sold with Infusomat Space, Outlook, and Vista pumps.
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 gravity and pump systems 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 medication leaks back into the patient's bloodstream.
The IV sets can allow medication from a secondary (piggyback) container to flow back into the primary IV container. This can cause medication to leak into the patient's bloodstream, potentially leading to incorrect dosing or infections. The sets also may not prime correctly, which could block the IV line and cause treatment interruptions.
Healthcare professionals using these IV sets with B Braun's Infusomat Space, Outlook, or Vista pumps are most at risk. Patients receiving IV treatments with these specific sets may also be affected.
Check for the model number NF1270A on the IV set. These sets were sold with B Braun's Infus: Infusomat Space, Outlook Pump, and Vista Basic Pump systems.
Look for the model number NF1270A on the IV set label to confirm it is affected.
The IV sets can cause medication to flow backward into the primary IV line and may not prime correctly, which could lead to incorrect dosing or infections.
Check the product label for the model number NF1270A. If it matches, stop using it with B Braun pumps and contact the manufacturer for a replacement.
Yes, these sets were used with B Braun's Infusomat Space, Outlook Pump, and Vista Basic Pump systems.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0643-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0643-2026 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.
