BEUDAMED
    FDA Adverse Event Summary report: N

    PROCEDURAL STRETCHER

    MDR report key: 3233722 · Received July 9, 2013

    Report

    Report Number
    1824206-2013-03413
    Date Received
    July 9, 2013
    Date of Event
    June 13, 2013
    Report Date
    June 13, 2013
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE BRAKE CASTERS ROLL AND SWIVEL WHILE IN BRAKE MODE. NO INJURY REPORTED. REF MFR # 3006697241-2013-00167.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    314181 PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8000

    Patients

    Seq Age Sex Outcome Treatment
    1