BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROCEDURAL STRETCHER

    MDR report key: 1810602 · Received August 10, 2010

    Report

    Report Number
    3006697241-2010-00008
    Event Type
    Malfunction
    Date Received
    August 10, 2010
    Date of Event
    July 19, 2010
    Report Date
    July 19, 2010
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE HEAD END OF THE SLEEP DECK WAS DRIFTING DUE TO THE HEAD CYLINDER LEAKING. THE TECHNICIAN REPLACED THE CYLINDER TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD HI/LOW HYDRAULIC CYLINDER IS LEAKING FLUID.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8000

    Patients

    Seq Age Sex Outcome Treatment
    1