BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRECISION®

    MDR report key: 2143221 · Received June 28, 2011

    Report

    Report Number
    3006630150-2011-00970
    Event Type
    Injury
    Date Received
    June 28, 2011
    Date of Event
    June 2, 2011
    Report Date
    June 2, 2011
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    030017
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ADDITIONAL INFORMATION RECEIVED STATED THAT THE PATIENT WILL NOT UNDERGO A POCKET REVISION AS SHE IS HAVING OTHER NON-DEVICE RELATED HEALTH ISSUES.

    Description of Event or Problem · 1

    A REPORT WAS RECEIVED THAT A PATIENT WILL UNDERGO A POCKET REVISION DUE TO DISCOMFORT.

    Description of Event or Problem · 1

    A REPORT WAS RECEIVED THAT A PATIENT WILL UNDERGO A POCKET REVISION DUE TO DISCOMFORT.

    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 62 YR Required Intervention