B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units include specific catalog numbers and pump models.
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 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 the IV system is not properly set up.
The IV sets can allow medication from secondary containers to flow back into the primary IV line, which may cause incorrect dosing or contamination. They also may not prime properly, leading to blockages that could cause medication to not flow as intended.
Healthcare professionals using these IV sets with gravity or pump systems, particularly those administering medications via piggyback infusions. Patients receiving IV treatments with these sets are at risk of incorrect dosing or infection.
Check for the catalog number 490367 on the IV set. These sets were sold with BBMI's Infusomat Space, Outlook, and Vista Basic pumps. The product label includes specific measurements and UDI-DI codes.
Look for the catalog number 490:367 on the IV set label to confirm if it is affected.
The sets can allow medication to flow backward from secondary containers into the primary IV line and may not prime properly, causing blockages or incorrect dosing.
The affected sets were used with BBMI's Infusomat Space, Outlook, and Vista Basic pumps.
Check for the catalog number 490367 on the IV set label, which is associated with the specific measurements and UDI-DI codes listed in the recall.
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-0662-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0662-2026 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.
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.
