Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1169-2025 — Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00

U.S. FDA — Device Enforcement · United States · 2023-06-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1169-2025
Date of alert
2023-06-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Murata Vios, Inc.
Product category
device
Product type
Devices
Reported risk: A premature failure condition was identified with the L2050R pulse oximeter SpO2 sensor that connects to the L2050G Vios chest sensor device. When a failure occurs, a Pulse Ox Sensor Off warning condition will be incorrectly displayed by the system.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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