BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1190551 · Received October 2, 2008

    Report

    Report Number
    1824206-2008-03676
    Event Type
    Malfunction
    Date Received
    October 2, 2008
    Date of Event
    September 8, 2008
    Report Date
    September 8, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE HILL-ROM TECHNICIAN INDICATED THE BEDS HEAD FUNCTION DID NOT WORK AND DID NOT HAVE AN ASSOCIATED ALARM. THE TECHNICIAN FOUND THE SOLENOID VALVE FOR THE HEAD DOWN WAS NOT FUNCTIONING. THE SOLENOID VALVE WAS REPLACED TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE BEDS HEAD UP FUNCTION DOES NOT WORK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE TOTAL CARE FNL HILL-ROM RITTER 1900

    Patients

    Seq Age Sex Outcome Treatment
    1