BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROCEDURAL STRETCHER

    MDR report key: 3172258 · Received May 17, 2013

    Report

    Report Number
    1824206-2013-02680
    Event Type
    Malfunction
    Date Received
    May 17, 2013
    Date of Event
    April 19, 2013
    Report Date
    April 19, 2013
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE TECH ALLEGED THE BRAKE CASTERS SWIVEL WHEN PUSHED WHILE IN BRAKE MODE. NO PT IMPACT. REFERENCE MFR REPORT NUMBER 3006697241-2013-00108.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    220050 PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8000

    Patients

    Seq Age Sex Outcome Treatment
    1