Murata Vios, Inc.: Device Recall

Recall #Z-1292-2025 · 08/09/2024

Class II: Risk

Recall Details

Recall Number: Z-1292-2025
Classification: Class II
Product Type: Device
Recalling Firm: Murata Vios, Inc.
Status: Ongoing
Date Initiated: 08/09/2024
Location: Woodbury, MN, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 50

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.

Product Description

Vios Monitoring System Bedside Monitor Model BSM2050

Distribution Pattern

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

Other Recalls by Murata Vios, Inc.

Class II: Risk 04/22/2024

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.

View all recalls by Murata Vios, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.