Official recall record

STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Cat (ref Z-3174-2024)

US FDA — Medical Devices · 2024-08-15 · United StatesClass II

Issuing authority: US FDA — Medical Devices
Alert date: 2024-08-15
Country of alert: United States
Alert level: Class II
Alert type: recall
Barcode (EAN/GTIN): 04046955348763
Brand on record: B Braun Medical Inc

What the authority reported

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

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: US FDA — Medical Devices · United States · all filters

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