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Hemodialysis Bloodlines

B. BRAUN MEDICAL INC. · Model SL-2010M2096 · UDI-DI 04046964367786

FJK Prescription
10
510(k) clearances
8,114
Adverse events (307 deaths)
36
Recalls
63
Facilities

Description

Streamline® Bloodline Set for Dialog+® Hemodialysis System

Recalls

DateFirmReason
2026-07-29Fresenius Medical Care Renal Therapies Group, LLCCommunication to recommend reviewing the IFU and ensuring that all treatment preparation and handling steps are performed as instructed.
2026-03-19B Braun Medical IncPotential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
2026-03-19B Braun Medical IncPotential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
2026-03-19B Braun Medical IncPotential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
2026-03-19B Braun Medical IncPotential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
2026-03-19B Braun Medical IncPotential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
2026-03-19B Braun Medical IncPotential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
2025-09-30B BRAUN MEDICAL INCThe potential for micro-air bubbles observed in the bloodline and air-in-line alarms due to damaged arterial and venous patient connectors.
2024-08-15B Braun Medical IncIncomplete insertion of the patient connector of the Streamline Airless System Hemodialysis Bloodline to the Locksite may result in the potential for occlusion during prograde rins
2024-08-15B Braun Medical IncIncomplete insertion of the patient connector of the Streamline Airless System Hemodialysis Bloodline to the Locksite may result in the potential for occlusion during prograde rin

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.