Murata Vios, Inc.: Medical Device Recall in 2025 - (Recall #: Z-1169-2025)

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, Software Version Numbers 1.54.20 and 1.56.00

Product Classification:

Class II

Date Initiated: June 6, 2023

Date Posted: February 19, 2025

Recall Number: Z-1169-2025

Event ID: 96133

Reason for Recall:

A premature failure condition was identified with the L2050R pulse oximeter SpO2 sensor that connects to the L2050G Vios chest sensor device. When a failure occurs, a Pulse Ox Sensor Off warning condition will be incorrectly displayed by the system.

Status: Ongoing

Product Quantity: 44 systems

Code Information:

All systems with Software Version Numbers 1.54.20 and 1.56.00 affected; UDI-DI: B595BSM20500

Distribution Pattern:

US Nationwide distribution in the state of NY.

Voluntary or Mandated:

Voluntary: Firm initiated