BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    MDR report key: 2840039 · Received November 15, 2012

    Report

    Report Number
    MW5027692
    Event Type
    Injury
    Date Received
    November 15, 2012
    Date of Event
    August 23, 2005
    Report Date
    October 31, 2012
    Manufacturer
    MEDTORNIC, INC.
    Product Code
    NEK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MS, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    BECAUSE OF THE MEDTRONIC INFUSE THAT WAS IMPLANTED IN ME DURING MY SURGERY, I NOW HAVE SEVERE PHYSICAL LIMITATIONS AND NOW SEE MY DOCTOR FREQUENTLY.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 48 YR Required Intervention