BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE SPO2RT

    MDR report key: 1892841 · Received November 3, 2010

    Report

    Report Number
    1824206-2010-10837
    Event Type
    Malfunction
    Date Received
    November 3, 2010
    Date of Event
    October 8, 2010
    Report Date
    October 10, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND ZERO VOLTAGE TO THE VALVE GUIDE TUBE. HE REPLACED THE HEAD UP SOLENOID VALVE TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO REC'D INDICATES THE HEAD OF THE BED WILL NOT RISE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE SPO2RT AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1