B Braun recalls STREAMLINE BLOODLINE SET for Dialog DR. Model SL-2010M2096A due to potential air bubble accumulation in arterial lines during hemodialysis. Affected units manufactured since June 9, 2025.
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
B Braun is recalling its STREAMLINE BLOODLINE SET for Dialog DR. Model SL-2010M2096A because air bubbles can accumulate in the arterial line during hemodialysis. This could cause complications for patients receiving dialysis treatments.
The tubing can trap small air bubbles when blood gases adhere to it under negative pressure during dialysis. This may cause blockages or complications in the arterial line.
Patients using hemodialysis treatments with this specific bloodline set are most at risk. The recall applies to units manufactured starting June 9, 2025.
Check for the model number SL-2010M2096A on the bloodline set. Affected units were manufactured starting June 9, 2025.
Look for the model number SL-2010M2096A on the bloodline set.
The recall is due to potential air bubble accumulation in the arterial line during hemodialysis, which could cause complications.
Model number SL-2010M2096A.
Units manufactured starting June 9, 2025.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-1798-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-1798-2026 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.
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