BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROCEDURAL STRETCHER

    MDR report key: 3161931 · Received April 19, 2013

    Report

    Report Number
    1824206-2013-03017
    Event Type
    Malfunction
    Date Received
    April 19, 2013
    Date of Event
    March 21, 2013
    Report Date
    March 21, 2013
    Manufacturer
    HILL-ROM DE MEXICO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    INFO INDICATED THE RIGHT HEAD SIDERAIL WOULD NOT LATCH. REFERENCE MFR REPORT NUMBER: 3006697241-2013-00090.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    171407 PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO 8000

    Patients

    Seq Age Sex Outcome Treatment
    1