BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON RECHARGEABLE IPG, 16-CHANNEL

    MDR report key: 1961090 · Received January 12, 2011

    Report

    Report Number
    1627487-2011-00060
    Event Type
    Injury
    Date Received
    January 12, 2011
    Date of Event
    April 16, 2010
    Report Date
    December 14, 2010
    Manufacturer
    ST JUDE MEDICAL - NEUROMODULATION DIVISION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    SJM HAS LIMITED INFO 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

    THE PT ((B)(6)) WAS IMPLANTED WITH AN IPG ON (B)(6) 2006. THE PROCEDURE OCCURRED IN THE UNITED STATES. ON (B)(6) 2010, IT WAS REPORTED THAT HER IPG WAS REPLACED WITH A SMALLER MODEL ON (B)(6) 2010 DUE TO ALLEGED DISCOMFORT. THE EXPLANTED DEVICE WILL BE RETURNED TO THE MANUFACTURER FOR ANALYSIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EON RECHARGEABLE IPG, 16-CHANNEL TOTALLY IMPLANTABLE PULSE GENERATOR LGW ST JUDE MEDICAL - NEUROMODULATION DIVISION 3716 56350

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention