BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2112896 · Received May 25, 2011

    Report

    Report Number
    1824206-2011-02893
    Event Type
    Malfunction
    Date Received
    May 25, 2011
    Date of Event
    May 5, 2011
    Report Date
    May 5, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THAT THE HEAD WILL NOT RAISE DUE TO SHORTING IN RIGHT INTERMEDIATE CABLE. REPLACED THE CABLE TO RESOLVE THIS ISSUE. BED FOUND IN THE MICU.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATED THAT THE HEAD WILL NOT RAISE WHEN OPERATED FROM RIGHT SIDERAIL. NO INJURIES ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P1900

    Patients

    Seq Age Sex Outcome Treatment
    1