BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    MDR report key: 2910225 · Received January 8, 2013

    Report

    Report Number
    MW5028506
    Event Type
    Injury
    Date Received
    January 8, 2013
    Date of Event
    January 2, 2008
    Report Date
    December 11, 2012
    Manufacturer
    MEDTRONIC, INC
    Product Code
    NEK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    BECAUSE OF THE MEDTRONIC INFUSE IMPLANTED DURING MY SURGERY, I'VE EXPERIENCED MANY SERIOUS PROBLEMS. INCLUDING PAIN, NERVE INJURIES, AS WELL AS A MENTAL ANGUISH THAT THINGS WILL NEVER GET BETTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    10221 MEDTRONIC INFUSE BONE GRAFT OR RHBMP2 MEDTRONIC INFUSE NEK MEDTRONIC, INC UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR Required Intervention| S