# FDA recall Z-3175-2024

> **B Braun Medical Inc** · Class II · device recall initiated 2024-08-15.

## Product

STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis.    Model/Catalog Number: SL-2000M2095DA

## 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.

## Key facts

- **Recall number:** Z-3175-2024
- **Recalling firm:** B Braun Medical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-15
- **Report date:** 2024-09-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bethlehem, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3175-2024

## Citation

> AI Analytics. FDA recall Z-3175-2024. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-3175-2024. Source: US FDA. Licensed CC0.

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