BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    MDR report key: 2896910 · Received December 19, 2012

    Report

    Report Number
    MW5028409
    Event Type
    Injury
    Date Received
    December 19, 2012
    Date of Event
    January 11, 2007
    Report Date
    December 12, 2012
    Manufacturer
    MEDTRONIC, INC.
    Product Code
    NEK
    Report Source
    Voluntary report
    Reporter Location
    FL, 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 NERVE INJURIES.

    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 44 YR Required Intervention| S