The Recall Desk
ModerateFDA (Devices)·Z-1292-2025·Announced 2025-03-12

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.

What this means for you

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
Hazard
Affected units
50

Distribution

Distributed nationwide across the United States.

The notice also names 7 states specifically:

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