BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SURGICAL STRETCHER

    MDR report key: 1971782 · Received January 13, 2011

    Report

    Report Number
    3006697241-2011-00004
    Event Type
    Malfunction
    Date Received
    January 13, 2011
    Date of Event
    December 14, 2010
    Report Date
    December 14, 2010
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN REPLACED THE BRAKE LEVEL AND THE LEFT HEAD BRAKE CASTER TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO REC'D INDICATES THE BRAKE ON THE STRETCHER IS FAULTY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SURGICAL STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8010

    Patients

    Seq Age Sex Outcome Treatment
    1