BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EON IPG

    MDR report key: 1930219 · Received November 18, 2010

    Report

    Report Number
    1627487-2010-03297
    Event Type
    Malfunction
    Date Received
    November 18, 2010
    Date of Event
    October 22, 2010
    Report Date
    October 22, 2010
    Manufacturer
    ST JUDE MEDICAL - NEUROMODULATION DIVISION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    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 RECEIVED HER SCS SYSTEM ON (B)(6) 2010. IT WAS REPORTED THAT SHE IS EXPERIENCING DIFFICULTY LOCATING THE IPG WITH THE CHARGING SYSTEM. EFFORTS TO RESOLVE THIS MATTER WITH THE USE OF A REPLACEMENT CHARGING SYSTEM PROVED UNSUCCESSFUL. X-RAYS OF THE PT'S SCS WERE TAKEN; HOWEVER, NO VISIBLE ABNORMALITIES WERE DETECTED. PLANS REGARDING SURGICAL INTERVENTION ARE PENDING. THIS REPORT IS BEING SUBMITTED AS A PRECAUTIONARY MEASURE AS SIMILARLY REPORTED EVENTS HAVE LED TO THE EXPLANT OF THE IPG.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EON IPG TOTALLY IMPLANTABLE PULSE GENERATOR LGW ST JUDE MEDICAL - NEUROMODULATION DIVISION 3716 3145876

    Patients

    Seq Age Sex Outcome Treatment
    1