B Braun recalls gravity IV sets with CARESITE injection sites due to potential medication backflow into primary IV containers and inability to prime. Affected units include specific catalog numbers and pump models.
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 gravity IV administration sets that can cause medication to flow backward into the main IV container and fail to prime properly. This could lead to incorrect dosing or infections if the sets are used without proper checks.
The sets may allow medication from secondary IV containers to flow back into the primary container, causing incorrect dosing. They also may not prime correctly, leading to blockages that could cause medication to not flow properly.
Healthcare professionals using these IV sets with B Braun's Infusomat pumps are most at risk. Patients receiving IV treatments with the recalled sets could face medication errors.
Check for catalog numbers 354202 or 354203 on the sets. These are used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps. The sets have two CARESITE injection sites.
Look for catalog numbers 354202 or 354203 on the IV sets.
The sets may allow medication to flow backward into the primary IV container and fail to prime properly, which could cause incorrect dosing or blockages.
The sets are used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Check for catalog numbers 354202 or 354203 on the IV sets, which have two CARESITE injection sites.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0625-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0625-2026 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.
