Class II
Medical Device Recall: Vios Monitoring System Bedside Monitor Model BSM2050
Murata Vios, Inc. · August 9, 2024
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.
Distribution
US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas.
States Affected
NATIONWIDE
Quantity Affected
50
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1292-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.