BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    MDR report key: 2896928 · Received January 3, 2013

    Report

    Report Number
    MW5028419
    Event Type
    Injury
    Date Received
    January 3, 2013
    Date of Event
    November 16, 2005
    Report Date
    November 28, 2012
    Manufacturer
    MEDTRONIC, INC
    Product Code
    NEK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    LA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    BECAUSE OF THE MEDTRONIC INFUSE THAT WAS IMPLANTED DURING MY SURGERY, I BEGAN TO EXPERIENCE SIGNIFICANT PAIN, AND IT HAS SERIOUSLY LIMITED MY PHYSICAL MOVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    3137 MEDTRONIC INFUSE BONE GRAFT OR RHBMP2 MEDTRONIC INFUSE NEK MEDTRONIC, INC UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Required Intervention