B Braun recalls STREAMLINE Bloodline Sets for potential occlusion during dialysis procedures. Incomplete connector insertion may cause flow restrictions, requiring switch to retrograde flow. Affected units have specific model numbers.
Incomplete insertion of the patient connector of the Streamline Airless System Hemodialysis Bloodline to the Locksite may result in the potential for occlusion during prograde rinseback procedures. If the patient connector is not fully inserted into the Locksite, the internal septum may not open fully enough to prevent restrictions to flow. may cause delays in therapy while clinicians are forced to switch to retrograde flow method
B Braun is recalling STREAMLINE Bloodline Sets used in hemodialysis for a risk of occlusion during procedures. If the patient connector isn't fully inserted, it may cause flow restrictions and require switching to a different method, delaying treatment.
The patient connector may not fully open if not inserted completely into the Locksite. This can restrict blood flow during prograde rinseback procedures, forcing clinicians to switch to retrograde flow which delays treatment.
Healthcare professionals using the STREAMLINE Bloodline Set for hemodialysis are most at risk. Patients receiving dialysis through this equipment could experience treatment delays.
Check for model number SL-2010M2096A on the product. The recall includes all unexpired lot numbers with UDI-DI 04046955674992.
Look for model number SL-2010M2096A on the STREAMLINE Bloodline Set.
The recall is for potential occlusion during hemodialysis procedures if the patient connector isn't fully inserted into the Locksite.
Incomplete insertion may cause flow restrictions, requiring a switch to retrograde flow which delays treatment.
Check for model number SL-2010M2096A and UDI-DI 04046955674992 on the product. All unexpired lot numbers are affected.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3179-2024 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-3179-2024 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.
