BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDTRONCI INFUSE BONE GRAFT OR RHBMP2

    MDR report key: 2892781 · Received December 26, 2012

    Report

    Report Number
    MW5028381
    Event Type
    Injury
    Date Received
    December 26, 2012
    Date of Event
    July 9, 2008
    Report Date
    December 6, 2012
    Manufacturer
    MEDTORNIC, INC.
    Product Code
    NEK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MS, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    BECAUSE THE MEDTRONIC INFUSE THAT WAS IMPLANTED INSIDE OF MY BACK, I BEGAN TO HAVE SERIOUS PROBLEMS. SOME OF THE PROBLEMS INCLUDE PAIN, MENTAL ANGUISH AND NERVE INJURIES.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 42 YR Required Intervention