BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2961161 · Received January 17, 2013

    Report

    Report Number
    1824206-2013-00486
    Event Type
    Malfunction
    Date Received
    January 17, 2013
    Date of Event
    January 7, 2013
    Report Date
    January 7, 2013
    Manufacturer
    HILL-ROM INC
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT REPLACED THE HEAD DOWN VALVE AND THE CARDIO PULMONARY RESUSCITATION VALVE AND THE ISSUE REMAINS. NO FURTHER INFO IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD SECTION WAS DRIFTING DOWN SLOWLY. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    25755 TOTALCARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC 1900

    Patients

    Seq Age Sex Outcome Treatment
    1