FDA recall Z-1292-2025

Murata Vios, Inc. · Class II · device

Product

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.

Distribution

US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas.

Key facts

Status: Ongoing
Initiation date: 2024-08-09
Report date: 2025-03-12
Voluntary/Mandated: Voluntary: Firm initiated
Location: Woodbury, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1292-2025