BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LAMITRODE 44

    MDR report key: 3961131 · Received July 15, 2014

    Report

    Report Number
    1627487-2014-26559
    Event Type
    Injury
    Date Received
    July 15, 2014
    Date of Event
    June 20, 2014
    Report Date
    June 26, 2014
    Manufacturer
    ST. JUDE MEDICAL- NEUROMODULATION
    Product Code
    GZB
    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 PATIENT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PATIENT'S HISTORY TO THE EVENT REPORTED. SJM DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

    Description of Event or Problem · 1

    IT WAS REPORTED THE PATIENT IS EXPERIENCING MUSCLE WEAKNESS IN HER RIGHT LEG. THE PATIENT STATED HER LEG IS WEAK BUT IT IS IMPROVING AND WAS ABLE TO AMBULATE. FURTHER FOLLOW UP IS PENDING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    413235 LAMITRODE 44 SCS LEAD GZB ST. JUDE MEDICAL- NEUROMODULATION 3262 4317676

    Patients

    Seq Age Sex Outcome Treatment
    1 46 YR Other SCS ANCHOR: MODEL 1194| IMPLANT DATE:| SCS IPG: MODEL 3788| IMPLANT DATE: