BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2072060 · Received April 21, 2011

    Report

    Report Number
    1824206-2011-02324
    Event Type
    Malfunction
    Date Received
    April 21, 2011
    Date of Event
    March 29, 2011
    Report Date
    March 29, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN DETERMINED THE PROBLEM TO BE A FAULTY VALVE GUIDE TUBE. HE REPLACED THE HEAD UP VALVE GUIDE TUBE TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE HEAD UP FUNCTION IS NOT WORKING. THE FUNCTION DOES NOT WORK MANUALLY OR UNDER POWER.

    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