Reported Sep 25, 2024 · Ongoing
STREAMLINE LONG-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis.…
B Braun Medical Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: B Braun Medical Inc · 824 12th Ave · Bethlehem, PA · 18018-3524
Is this the product you have?
- STREAMLINE LONG-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis
- Model/Catalog NumberSL-2000M2095W
- Lot codes and dates
- UDI-DI 04046955348800; All Unexpired Lot Numbers
- Amount recalled
- 142336 units
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
- Nationwide
Why it was 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
This product could cause temporary or reversible health problems — stop using it.
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