BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    MDR report key: 2854813 · Received November 27, 2012

    Report

    Report Number
    MW5027759
    Event Type
    Injury
    Date Received
    November 27, 2012
    Date of Event
    November 13, 2008
    Report Date
    October 1, 2012
    Manufacturer
    MEDTRONIC, INC.
    Product Code
    NEK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    BECAUSE OF THE MEDTRONIC INFUSE USED ON MY BACK DURING SURGERY, I NOW HAVE EXTREME PAIN, AND I HAVE TO FREQUENTLY VISIT MY DOCTOR BECAUSE OF IT.

    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 38 YR Required Intervention