BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    MDR report key: 2840001 · Received November 15, 2012

    Report

    Report Number
    MW5027679
    Event Type
    Injury
    Date Received
    November 15, 2012
    Date of Event
    September 25, 2007
    Report Date
    November 5, 2012
    Manufacturer
    MEDTRONIC INC.
    Product Code
    NEK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    BECAUSE MY SURGEON IMPLANTED THE MEDTRONIC INFUSE DURING MY SURGERY. I NOW AM CONSTANTLY WORRIED ABOUT HAVING TO GO BACK UNDER. I AM IN A LOT OF PAIN.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 32 YR Required Intervention