BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    MDR report key: 2935584 · Received January 25, 2013

    Report

    Report Number
    MW5028782
    Event Type
    Injury
    Date Received
    January 25, 2013
    Date of Event
    July 25, 2002
    Report Date
    December 26, 2012
    Manufacturer
    MEDTRONIC, INC.
    Product Code
    NEK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WI, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    MY SURGEON USED THE MEDTRONIC INFUSE, WHICH CAUSED ME SIGNIFICANT PAIN. A DIAGNOSIS OF CANCER, AS WELL AS MENTAL ANGUISH. I'M CONSTANTLY WORRIED THINGS WILL NEVER GET BETTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    36224 MEDTRONIC INFUSE BONE GRAFT OR RHBMP2 MEDTRONIC INFUSE SOFAMOR NEK MEDTRONIC, INC. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR Hospitalization| L| R| S