Murata Vios, Inc.: Medical Device Recall in 2025 - (Recall #: Z-1292-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Vios Monitoring System Bedside Monitor Model BSM2050

Product Classification:

Class II

Date Initiated: August 9, 2024

Date Posted: March 12, 2025

Recall Number: Z-1292-2025

Event ID: 96252

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.

Status: Ongoing

Product Quantity: 50

Code Information:

1.56.01 UDI: +B595BSM20500/$$7V1.56.01/16D20230630S 1.57.20 UDI: +B595BSM20500/$$7V1.57.20/16D20231129Y Software Versions 1.56.01 and 1.57.20

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated