BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STANDARD STRETCHER

    MDR report key: 3250476 · Received July 23, 2013

    Report

    Report Number
    1824206-2013-03628
    Event Type
    Malfunction
    Date Received
    July 23, 2013
    Date of Event
    June 27, 2013
    Report Date
    June 27, 2013
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    PA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE SIDE RAIL WOULD NOT LATCH. NO REPORT OF INJURY. REF MFR REPORT 3006697241-2013-00182.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    341893 STANDARD STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8005

    Patients

    Seq Age Sex Outcome Treatment
    1