B Braun recalls STREAMLINE FRESENI: Tubing for hemodialysis that may cause blood flow blockage if not properly connected, risking treatment delays. Affected units have specific model numbers and lot 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 FRESENIUS tubing used in hemodialysis that may cause blood flow blockages if not fully inserted into the Locksite. This could lead to treatment delays and require switching to a less efficient retrograde flow method.
If the patient connector isn't fully inserted into the Locksite, the internal septum may not open properly. This can restrict blood flow during prograde rinseback procedures, causing delays in treatment and forcing a switch to retrograde flow.
Patients undergoing hemodialysis and healthcare providers using the tubing. Those most at risk are clinicians who may not fully insert the connector during procedures.
Check for model number SL-2000M2095DA, UDI-DI 04046955776023, and all unexpired lot numbers. The tubing is used to transfer blood between patients and hemodialysis machines.
Ensure the patient connector is fully inserted into the Locksite before use to prevent flow restrictions.
The tubing may cause blockages if not properly connected, so it's recommended to check the connection before use.
Model/Catalog Number: SL-2000M2095DA; UDI-DI 04046955776023; All unexpired lot numbers.
No, but you should check the connection before use to prevent flow restrictions.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3175-2024 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-3175-2024 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.
