B. Braun recalls STREAMLINE BLOODLINE SET FOR DIALOG (model SL-2010M2096) due to potential micro-air bubbles in bloodlines causing alarm errors. Affected units include specific lot numbers listed in the recall.
The potential for micro-air bubbles observed in the bloodline and air-in-line alarms due to damaged arterial and venous patient connectors.
B. Braun is recalling certain hemodialysis bloodline sets that may have damaged connectors, potentially causing micro-air bubbles in the bloodline and air-in-line alarms. This could lead to inaccurate alarms during dialysis treatments, which is a serious risk for patients.
Damaged arterial and venous patient connectors in the bloodline set can allow micro-air bubbles to form in the bloodline. This may cause the air-in-line alarms to trigger incorrectly, potentially leading to unsafe dialysis conditions.
Patients using hemodialysis treatments with the recalled bloodline sets are most at risk. The recall affects specific model numbers and lot numbers sold between 2024 and 2026.
Check for the model number SL-2010M2096 on the product. Affected units include specific lot numbers listed in the recall notice, such as A2500119 through A2500357.
Identify the model number (SL-2010M2096) and lot numbers on the bloodline set.
Reach out to B. Braun Medical Inc for guidance on whether your specific unit is affected and next steps.
The model number is SL-2010M2096.
Affected lot numbers include A2500119 through A2500357, as listed in the recall notice.
The recall is due to potential micro-air bubbles in the bloodline and air-in-line alarms caused by damaged arterial and venous patient connectors.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0070-2026 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-0070-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
