BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1190557 · Received October 2, 2008

    Report

    Report Number
    1824206-2008-03680
    Event Type
    Malfunction
    Date Received
    October 2, 2008
    Date of Event
    September 3, 2008
    Report Date
    September 3, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE FACILITIES ENGINEER INDICATED THE HI/LOW FUNCTION OF THE BED IS DRIFTING DOWN. THE FACILITIES ENGINEER IS CURRENTLY WORKING TO DETERMINE THE CAUSE OF THE HI/LOW DRIFT. THERE IS NO RESOLUTION AT THIS TIME.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE HEAD HI/LOW FUNCTION OF THE BED IS DRIFTING DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED HOSP BED FNL HILL-ROM RITTER 1900

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK