Murata Vios, Inc. has recalled approximately 50 Vios Monitoring System Bedside Monitors (Model BSM2050) running software versions 1.56.01 and 1.57.20. The recall was issued because the monitor's batteries may deplete over time if the devices are stored for long periods without being plugged into a wall outlet. If the battery becomes fully depleted, it can cause the bedside monitor to lose its connection to the system tablet.
A loss of connectivity between the bedside monitor and the system tablet could prevent healthcare providers from seeing real-time patient data or receiving important alerts. No incidents or injuries have been reported to date.
Quantity affected: 50 units.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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