BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1890714 · Received November 1, 2010

    Report

    Report Number
    1824206-2010-10787
    Event Type
    Malfunction
    Date Received
    November 1, 2010
    Date of Event
    October 6, 2010
    Report Date
    October 6, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND A FAULTY VALVE GUIDE TUBE. THE TECHNICIAN REPLACED THE HEAD UP VALVE GUIDE TUBE TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES, THE HEAD UP FUNCTION NOT WORKING. THE FUNCTION DOES NOT WORK MANUALLY OR UNDER POWER AND THE BATTERY LED IS ON.

    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