BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    MDR report key: 2896927 · Received January 3, 2013

    Report

    Report Number
    MW5028418
    Event Type
    Injury
    Date Received
    January 3, 2013
    Date of Event
    October 5, 2007
    Report Date
    December 20, 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

    I HAD THE INFUSE IMPLANTED INSIDE OF ME DURING BACK SURGERY AND I SUFFERED SERIOUS INJURY INCLUDING PAIN AND THE NEED TO HAVE ANOTHER SURGERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2877 MEDTRONIC INFUSE BONE GRAFT OR RHBMP2 MEDTRONIC INFUSE NEK MEDTRONIC, INC UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 28 YR Required Intervention