Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
STREAMLINE BLOODLINE SET FOR DIALOG-Tubing to be used to transfer Recalled by B Braun Medical Inc Due to Incomplete insertion of the patient connector of the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact B Braun Medical Inc directly.
Affected Products
STREAMLINE BLOODLINE SET FOR DIALOG-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2010M2096
Quantity: 9864165 units
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About B Braun Medical Inc
B Braun Medical Inc has 148 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report