B Braun recalls specific IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units include US1295 models with catalog number 352:352394.
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 contamination of the medication.
The IV sets can allow medication from a secondary container to flow back into the primary container, which may cause incorrect dosing or contamination. They also may not prime correctly, leading to blockages or incomplete medication delivery.
Healthcare professionals using these IV sets with B Braun pumps or gravity systems are most at risk. Patients receiving IV treatments with the recalled sets may also be affected.
Check for the US1295 ULTRASITE IV ADMIN SET 60DROP label with catalog number 352394. These sets were sold with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Look for the US1295 ULTRASITE IV ADMIN SET 60DROP label with catalog number 352394.
The sets can cause medication to flow backward into the primary container and fail to prime properly, which may lead to incorrect dosing or contamination.
The sets were used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Check for the US1295 ULTRASITE IV ADMIN SET 60DROP label with catalog number 352394.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0644-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0644-2026 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.
