Recall Atlas

Murata Vios recalls

4 official recalls and safety alerts involving Murata Vios since 2025-01, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Murata Vios or the relevant agency.

  1. 2025-03-12
  2. US
    Drugs & medicalClass II

    Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor Model BSM2050

    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.

    FDA · DeviceMurata Vios, Inc.US Nationwide distribution in the states of Florida, Louisiana, Maryland,…Official notice →
  3. 2025-02-19
  4. US
    Drugs & medicalClass II

    Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00

    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…

    FDA · DeviceMurata Vios, Inc.US Nationwide distribution in the state of NY.Official notice →
  5. 2025-02-05
  6. US
    Drugs & medicalClass II

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

    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…

    FDA · DeviceMurata Vios, Inc.Worldwide - US Nationwide distribution in the states of NY, TX, OH, MD and the…Official notice →
  7. 2025-01-22
  8. US
    Drugs & medicalClass II

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

    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…

    FDA · DeviceMurata Vios, Inc.Worldwide - US Nationwide distribution in the states of NY, LA and the country…Official notice →