B Braun 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 is recalling certain IV administration sets used with gravity and pump 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 complications if the set is not used correctly.
The IV sets can allow medication from a secondary container to flow back into the primary container, which may cause incorrect dosing. They also may not prime correctly, leading to blockages or incomplete medication delivery.
Healthcare professionals and patients using IV therapy with gravity or pump systems. Those using the specific recalled sets are most at risk.
Check for the catalog number 490301 or the UDI-DI 04046964716867 on the set. These sets were sold with BBMI's Infusomat Space, Outlook, and Vista Basic pumps.
Look for the catalog number 490301 or UDI-DI 04046964716867 on the IV set.
The sets can cause medication to flow backward into the primary container and fail to prime properly, which may lead to incorrect dosing or blockages.
Check for the catalog number 490301 or UDI-DI 04046964716867 on the IV set, which was sold with BBMI's Infusomat Space, Outlook, and Vista Basic pumps.
The recall record does not specify a remedy, so contact B Braun Medical Inc for guidance.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0703-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0703-2026 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.
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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.
