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Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00
Recalled February 19, 2025 · FDA recall Z-1169-2025 · Murata Vios
Hazard
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. · FDA Class II
Units
44 systems
Sold at
US Nationwide distribution in the state of NY.
Description
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.
Product
Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00
Manufacturer(s)
Murata Vios, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →