FDAAugust 9, 2024device
Vios Monitoring System Bedside Monitor Model BSM2050
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Batteries may deplete over time while not in use if devices are stored without being plugged in to wall outlet. Depleted batteries may lead to tablet connectivity issues.
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.
- FDAmuRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate2024-04-22
- FDAVios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.002023-06-06
- FDAmuRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate2021-06-21
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