B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and expiration dates.
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 IV administration sets used in gravity and pump IV systems because they can cause medication to flow backward into the main container and fail to prime properly. This could lead to incorrect dosing or contamination of the medication.
The IV sets can allow medication from secondary containers to flow back into the primary container, which may cause incorrect dosing or contamination. They also fail to prime properly, leading to blockages in the system.
Healthcare professionals using these IV sets with gravity or pump systems are most at risk. Patients receiving IV treatments with the recalled sets could be affected if the sets are used incorrectly.
Check for the catalog number 49050: 490507. The sets were sold with specific expiration dates and are used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Look for the catalog number 490507 on the IV set packaging or label.
Reach out to B Braun Medical for assistance with the recall if you have the catalog number 490507.
The IV sets can cause medication to flow backward from secondary containers into primary containers and fail to prime properly, leading to incorrect dosing or contamination.
The recall affects IV sets used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Check for the catalog number 490507 on the IV set label or packaging. The sets have specific expiration dates and are used with the mentioned pumps.
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-0674-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0674-2026 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.
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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.
