Vios bedside monitor batteries may deplete during storage
Murata Vios bedside monitors may experience battery depletion if stored without power, causing tablet connectivity issues. Affected units should be kept plugged in while in storage.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II device recall with no reported illnesses, injuries, or hospitalizations. The hazard is functional degradation through battery depletion during storage, which is preventable through proper device storage practices.
Plain-English summary
Murata Vios, Inc. is recalling the Vios Monitoring System Bedside Monitor Model BSM2050 (50 units affected). The device may experience battery depletion and subsequent connectivity issues.
When bedside monitors are stored without being plugged into a wall outlet, batteries may deplete over time. This depletion can lead to tablet connectivity issues when the device is deployed for clinical use.
The recall affects units distributed nationwide in Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas. Consumers and healthcare facilities should ensure affected monitors remain plugged in during storage to maintain battery charge and device functionality.
The recalled product
- Product
- Vios Monitoring System Bedside Monitor Model BSM2050
- Manufacturer
- Murata Vios, Inc.
- Category
- Medical Device
- Affected units
- 50
Distribution
Related recalls
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Similar recalls
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FDA (Devices) · 2025-02-19
- HighBedside cardiac monitor system recalled for display distortion
FDA (Devices) · 2025-02-05
- HighMurata Vios Cardiac Monitor Model 2050 Displays Distorted and Flickering Waveforms
FDA (Devices) · 2025-01-22
- HighMonitor batteries recalled because they can lose the ability to charge
FDA (Devices) · 2025-11-19
- HighPatient monitors recalled over batteries that can lose backup power
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