Class II
Medical Device Recall: Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00
Murata Vios, Inc. · June 6, 2023
Reason for Recall
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.
Distribution
US Nationwide distribution in the state of NY.
States Affected
NATIONWIDE
Quantity Affected
44 systems
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1169-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.