BEUDAMED
    FDA Adverse Event Other Summary report: N

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    MDR report key: 2915763 · Received January 10, 2013

    Report

    Report Number
    MW5028538
    Event Type
    Other
    Date Received
    January 10, 2013
    Date of Event
    November 16, 2009
    Report Date
    December 26, 2012
    Manufacturer
    MEDTRONIC, INC.
    Product Code
    NEK
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    BECAUSE OF THE MEDTRONIC INFUSE THAT WAS IMPLANTED DURING MY SURGERY, I BEGAN TO SUFFER FROM SERIOUS PROBLEMS INCLUDING PAIN, CANCER, MENTAL ANGUISH AS WELL AS PHYSICAL LIMITATIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    15804 MEDTRONIC INFUSE BONE GRAFT OR RHBMP2 MEDTRONIC INFUSE NEK MEDTRONIC, INC. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1