FDAJune 6, 2023device
Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00
Official recall recorded by the U.S. Food & Drug Administration.
The 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.
What to do
FDA enforcement status: Ongoing
Brands named
murata viosmurata
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAVios Monitoring System Bedside Monitor Model BSM20502024-08-09
- FDAmuRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate2024-04-22
- FDAmuRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate2021-06-21
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