BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRECISION

    MDR report key: 2000973 · Received February 18, 2011

    Report

    Report Number
    3006630150-2011-00252
    Event Type
    Injury
    Date Received
    February 18, 2011
    Date of Event
    January 12, 2011
    Report Date
    January 12, 2011
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P030017
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    ADDITIONAL INFORMATION RECEIVED STATED THAT THE PATIENT HAD A LEAD REVISION PROCEDURE DUE TO INADEQUATE STIMULATION. THE PATIENT IS REPORTEDLY DOING WELL FOLLOWING THE PROCEDURE.

    Description of Event or Problem · 1

    A REPORT THAT A PATIENT WILL UNDERGO AN IPG REVISION FOR REASONS UNKNOWN WAS RECEIVED.

    Description of Event or Problem · 1

    A REPORT THAT A PATIENT WILL UNDERGO AN IPG REVISION FOR REASONS UNKNOWN WAS RECEIVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRECISION SPINAL CORD STIMULATOR LGW BOSTON SCIENTIFIC NEUROMODULATION SC-1110-02 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR Required Intervention