# FDA recall Z-1169-2025

> **Murata Vios, Inc.** · Class II · device recall initiated 2023-06-06.

## Product

Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00

## 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.

## Distribution

US Nationwide distribution in the state of NY.

## Key facts

- **Recall number:** Z-1169-2025
- **Recalling firm:** Murata Vios, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-06-06
- **Report date:** 2025-02-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Woodbury, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1169-2025

## Citation

> AI Analytics. FDA recall Z-1169-2025. Retrieved 2026-09-22 from https://api.ai-analytics.org/recall/Z-1169-2025. Source: US FDA. Licensed CC0.

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