BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 2921759 · Received January 14, 2013

    Report

    Report Number
    1627487-2013-03111
    Event Type
    Injury
    Date Received
    January 14, 2013
    Date of Event
    December 23, 2012
    Report Date
    December 23, 2012
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    SJM HAS LIMITED INFORMATION RELATED TO THE PT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PT'S HISTORY TO THE EVENT REPORTED. SJM DEFERS TO THE PT'S PHYSICIAN REGARDING MEDICAL HISTORY.

    Description of Event or Problem · 1

    DEVICE 1 OF 2. REFERENCE MFR REPORT: 1627487-2013-03112. IT WAS REPORTED THE PT WENT TO THE EMERGENCY ROOM DUE TO POST-OPERATIVE PAIN. F/U IDENTIFIED THERE WAS NO INFECTION OR SUSPICION OF INFECTION. IT WAS ALSO REPORTED PER THE PT, THE SURGICAL PAIN HAS SIGNIFICANTLY REDUCED AND IS IMPROVING DAILY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    19942 EON MINI SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 3856855

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Required Intervention