B Braun recalls STREAMLINE Long-Tubing for hemodialysis use due to potential blood flow blockage if patient connector isn't fully inserted. Affected units have model SL-2:000M2095W. Contact for remedy.
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 Long-Tubing used in hemodialysis treatments because improper insertion of the patient connector can cause blood flow blockages. This may delay treatment and require switching to a less effective method. The recall affects all unexpired units with the model number SL-2000M2095W.
If the patient connector isn't fully inserted into the Locksite, the internal septum may not open completely. This can restrict blood flow during dialysis, potentially causing delays in treatment and requiring a switch to retrograde flow method.
Healthcare providers using hemodialysis equipment are most at risk. Patients receiving dialysis treatments may experience delays in therapy if the tubing is not properly connected.
Check for model number SL-2000M2095W on the tubing. The recall applies to all unexpired units with this model and UDI-DI 04046955348800.
Look for model number SL-2000M2095W on the tubing to confirm if it's affected.
The recall is due to potential blood flow blockages if the patient connector isn't fully inserted into the Locksite during dialysis procedures.
The recall record does not specify a remedy, so contact B Braun Medical Inc for further instructions.
The tubing may be safe if the patient connector is fully inserted, but improper use can cause delays in treatment.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3177-2024 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-3177-2024 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.
