Z-3179-2024 Class II Ongoing
FDA device recall Z-3179-2024 was initiated by B Braun Medical Inc on Aug 15, 2024 and is designated Class II. 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… The recall status is ongoing. Affected quantity: 11262112 units.
Recall Details
- Product Type
- Devices
- Report Date
- Sep 25, 2024
- Initiation Date
- Aug 15, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 11262112 units
Product Description
STREAMLINE BLOODLINE SET FOR DIALOG DR-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2010M2096A
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 Pattern
US Nationwide distribution.
Code Information
UDI-DI 04046955674992; All Unexpired Lot Numbers
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-3179-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026