B Braun recalls ULTRASITE IV sets used with Infusomat pumps 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 ULTRASITE IV administration sets used with Infusomat pumps 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 not addressed.
The ULTRASITE sets can allow medication from a secondary IV container to flow back into the primary IV container. This can cause incorrect dosing or contamination. The sets also may not prime correctly, leading to blockages or incomplete medication delivery.
Healthcare professionals using these IV sets with Infusomat pumps are most at risk. Patients receiving IV treatments with the recalled sets could be affected if the sets are not properly managed.
Check for catalog numbers 352049-C or 375100-C on the sets. These units were sold with Infusomat pumps like the Space, Outlook, or Vista Basic models. The expiration date is the earliest of component expiration or 60 months from manufacture.
Look for catalog numbers 352049-C or 375100-C on the ULTRASITE IV sets.
Reach out to B Braun Medical Inc for further assistance or to confirm if your set is affected.
The ULTRASITE sets can cause medication to flow backward into the primary IV container and may not prime correctly, leading to incorrect dosing or blockages.
The recalled sets are used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump.
Check for catalog numbers 352049-C or 375100-C on the sets. These units were sold with specific Infusomat pump models and have expiration dates based on component expiration or 60 months.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0714-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0714-2026 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.
