PlainRecalls
FDA Devices Moderate Class II Ongoing

Vios Monitoring System Bedside Monitor Model BSM2050

Reported: March 12, 2025 Initiated: August 9, 2024 #Z-1292-2025

Product Description

Vios Monitoring System Bedside Monitor Model BSM2050

Reason for Recall

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.

Details

Recalling Firm
Murata Vios, Inc.
Units Affected
50
Distribution
US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas.
Location
Woodbury, MN

Frequently Asked Questions

What product was recalled?
Vios Monitoring System Bedside Monitor Model BSM2050. Recalled by Murata Vios, Inc.. Units affected: 50.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 12, 2025. Severity: Moderate. Recall number: Z-1292-2025.