# FDA recall Z-0956-2025

> **Murata Vios, Inc.** · Class II · device recall initiated 2021-06-21.

## Product

muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate

## Reason for recall

During the set-up and workflow to begin Vios monitoring, it has been noticed that patient vital signs and ECG waveforms can become distorted and will flicker or flash very fast. This issue only occurs on the Central Station Monitor (CSM) in the patient tiles view and is not seen at any other point during patient monitoring & not on the Bedside Monitor.

## Distribution

Worldwide - US Nationwide distribution in the states of NY, LA and the country of India.

## Key facts

- **Recall number:** Z-0956-2025
- **Recalling firm:** Murata Vios, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2021-06-21
- **Report date:** 2025-01-22

- **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-0956-2025

## Citation

> AI Analytics. FDA recall Z-0956-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0956-2025. Source: US FDA. Licensed CC0.

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