# FDA recall Z-1292-2025

> **Murata Vios, Inc.** · Class II · device recall initiated 2024-08-09.

## 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

- **Recall number:** Z-1292-2025
- **Recalling firm:** Murata Vios, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-09
- **Report date:** 2025-03-12

- **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-1292-2025

## Citation

> AI Analytics. FDA recall Z-1292-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1292-2025. Source: US FDA. Licensed CC0.

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