Braun Medical recalls Streamline tubing for hemodialysis due to risk of flow restrictions from incomplete connector insertion. Affected units have specific model numbers and lot numbers. 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
Braun Medical is recalling Streamline tubing used in hemodialysis treatments because if the patient connector isn't fully inserted into the Locksite, it can cause flow restrictions. This may force clinicians to switch to a less efficient retrograde flow method, delaying treatment.
The patient connector may not fully open if not completely inserted into the Locksite, causing restrictions in blood flow during hemodialysis. This can lead to delays in treatment as clinicians may need to switch to a retrograde flow method.
Hemodialysis patients and their healthcare providers who use the Streamline tubing. Those with the specific model number SL-2000M2095D are most at risk.
Check for model number SL-2000M2095D on the tubing. The tubing is used in hemodialysis to transfer blood between patients and hemodialyzers. All unexpired lot numbers are affected.
Look for model number SL-2000M2095D on the tubing to confirm if it's affected.
Reach out to Braun Medical for guidance on next steps if the tubing is affected.
The tubing may cause flow restrictions if the patient connector isn't fully inserted into the Locksite, potentially delaying hemodialysis treatments.
Model number SL-2000M2095D.
The recall does not require immediate stop use; however, affected units should be checked and contacted for guidance.
We’ve drafted a message you can send Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-3174-2024 — Braun Medical Braun Medical Hello, I own a Braun Medical that is covered by recall Z-3174-2024 from Braun Medical. 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.
