BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    MDR report key: 2840004 · Received November 15, 2012

    Report

    Report Number
    MW5027681
    Event Type
    Injury
    Date Received
    November 15, 2012
    Date of Event
    January 30, 2012
    Report Date
    October 31, 2012
    Manufacturer
    MEDTORNIC, INC.
    Product Code
    NEK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    BECAUSE OF THE MEDTRONIC INFUSE IMPLANTED IN MY BACK I BEGAN TO HAVE SERIOUS PROBLEMS INCLUDING PAIN, MENTAL ANGUISH AND FEAR OF UNDERGOING ANOTHER SURGERY.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Required Intervention