B Braun Medical recalls 50+ IV administration sets used with gravity and pump systems due to potential backflow of medication and inability to prime. Check catalog numbers listed for affected 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 50 different IV administration sets that can cause medication to flow backward into the main IV line or become blocked, which could lead to incorrect dosing or infection. These sets are used with gravity IV systems and certain pumps like the Infusomat Space.
The IV sets can allow medication from a secondary (piggyback) container to flow back into the primary IV container, and they may not prime properly (become blocked). This could cause incorrect medication dosing or infection if the backflow introduces contaminants.
Healthcare professionals and patients using IV therapy with gravity systems or specific pumps (Infusomat Space, Outlook, Vista Basic) who have the recalled sets. Those with the listed catalog numbers are most at risk.
Check the catalog number on the product label. Affected models include 50 specific IV sets with catalog numbers from 352636 to 490658 as listed in the recall notice.
Look for the catalog number on the IV set label to confirm if it's affected. The recall includes 50 specific models with catalog numbers listed in the notice.
If you have an affected set, contact B Braun Medical directly for instructions on how to return or replace it.
The recall states these sets can cause backflow or blockage, so they should not be used until replaced with a safe model.
These sets are used with specific pumps like Infusomat Space, Outlook, and Vista Basic, but the recall does not list all affected pumps.
Check the catalog number on the product label. The recall lists 50 specific catalog numbers that are affected.
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-0670-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0670-2026 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.
