BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OBGYN STRETCHER

    MDR report key: 1971783 · Received January 13, 2011

    Report

    Report Number
    3006697241-2011-00003
    Event Type
    Malfunction
    Date Received
    January 13, 2011
    Date of Event
    December 15, 2010
    Report Date
    December 15, 2010
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    REPAIRS HAVE NOT BEEN COMPLETED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD SECTION WOULD NOT FULLY LOWER AND WOULD STAY UP A FEW INCHES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OBGYN STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8050

    Patients

    Seq Age Sex Outcome Treatment
    1