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 457515.
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 or pump systems because they might let medication flow backward into the main container and not prime properly. This could lead to incorrect dosing or infections if the sets are used without proper checks.
The sets might allow medication from secondary IV containers to flow back into the primary container, which could cause incorrect dosing or infections. They also may not prime correctly, leading to blockages that prevent proper medication delivery.
Healthcare professionals using these IV sets with B Braun pumps like Infusomat Space, Outlook, or Vista Basic are most at risk. Patients receiving IV treatments with these sets could be affected if the sets are not properly checked.
Check for the catalog number 457515 on the set. These sets were sold with B Braun pumps including Infusomat Space, Outlook, and Vista Basic models.
Look for the catalog number 457515 on the IV set label to confirm it is affected.
The recall is due to potential backflow of medication from secondary IV containers into primary containers and the inability to prime the sets, which could lead to incorrect dosing or infections.
Check the set label for catalog number 457515. If affected, stop using it and contact B Braun for further instructions.
These sets were used with B Braun pumps including Infusomat Space, Outlook, and Vista Basic models.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0651-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0651-2026 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.
