BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2100233 · Received May 16, 2011

    Report

    Report Number
    1824206-2011-02721
    Event Type
    Malfunction
    Date Received
    May 16, 2011
    Date of Event
    April 25, 2011
    Report Date
    April 25, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN ISOLATED THE ISSUE TO THE RIGHT SIDERAIL UCM CIRCUIT BOARD. HE REPLACED THE CIRCUIT BOARD TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES WHEN THE BED IS PLUGGED IN THE SOLENOIDS WILL CLICK AND THE HI/LOW FUNCTION WILL TRY TO GO UP THEN DOWN WITHOUT PUSHING THE BUTTON.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1