BEUDAMED
    FDA Recall Open, Classified

    Vios Monitoring System Bedside Monitor Model BSM2050

    Recall: Z-1292-2025 · Initiated August 9, 2024

    Recall

    Recall Number
    Z-1292-2025
    Event Number
    96252
    Firm
    Murata Vios, Inc.
    FEI Number
    3015328411
    Product Code
    DRT
    Status
    Open, Classified
    Root Cause
    Labeling design
    Initiated
    August 9, 2024
    Posted
    March 6, 2025
    Address
    700 Commerce Dr, Ste 190, Woodbury, MN, 55125-9239

    Description

    Vios Monitoring System Bedside Monitor Model BSM2050

    Reason

    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.

    Action

    The firm sent a single page of instructions to customers on August 9, 2024 via email. Customers were informed that tablets should remain plugged into a wall outlet when the tablet is not in use. The tablet battery should not be allowed to fully deplete at any time during patient monitoring or when not in use.

    Distribution

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

    Quantity

    50