Medical Device Recall: SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095
B Braun Medical Inc · August 15, 2024
Reason for Recall
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
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
10658351 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3173-2024
Status: ongoing
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