B Braun recalls CARESAFE IV administration sets used with Infusomat pumps due to potential medication backflow and inability to prime, which could cause serious injury during IV therapy.
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun is recalling specific CARESAFE IV administration sets used with their Infusomat pumps because they might allow medication to flow backward into the main IV line and become clogged, risking serious injury during IV treatments.
These sets can allow medication from a secondary IV container to flow back into the primary IV line. They may also become clogged (occluded) when trying to prime the set, which could lead to serious injury if medication flows back into the patient.
Healthcare professionals using these sets with Infusomat pumps for IV therapy are most at risk. Patients receiving IV treatments with these specific sets could be affected.
Check for the following catalog numbers: 354302-354310. These sets are labeled with specific lengths (104 in., 110 in., 114 in., 134 in.) and are used with B Braun's Infusomat Space pumps.
Immediately stop using the recalled CARESAFE IV administration sets if you have them.
Reach out to B Braun Medical Inc for guidance on replacement or alternative solutions.
These sets can allow medication to flow backward into the primary IV line and become clogged when trying to prime, which could cause serious injury during IV therapy.
The affected models have catalog numbers 354302 through 354310, with specific lengths (104 in., 110 in., 114 in., 134 in.) and are used with B Braun's Infusomat Space pumps.
Check the catalog number on the set or look for the specific lengths (104 in., 110 in., 114 in., 134 in.) and ensure it's used with B Braun's Infusomat Space pumps.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0623-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0623-2026 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.
