B Braun recalls specific IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units have catalog number 490:225.
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 the set is used without proper checks.
The IV set may allow medication from a secondary container to flow back into the primary container during use. This can cause incorrect dosing or contamination if the set cannot be properly primed to check for blockages.
Healthcare professionals using these IV sets with B Braun's Infusomat, Outlook, or Vista pumps are most at risk. Patients receiving IV treatments with the recalled sets could face medication errors.
Check for the catalog number 490225 on the set. These sets were sold with B Braun's Infusomat, Outlook, or Vista pumps between 2020 and 2024 (based on expiration dates).
Look for the catalog number 490225 on the IV administration set.
Reach out to B Braun Medical Inc for guidance on safe use or replacement options.
The catalog number is 490225.
No, but you should check if your set has the catalog number 490225 and contact B Braun for advice.
The recall affects IV sets used with B Braun's Infusomat, Outlook, and Vista Basic 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-0704-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0704-2026 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.