BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LINEAR ST

    MDR report key: 19106399 · Received April 15, 2024

    Report

    Report Number
    3006630150-2024-02368
    Event Type
    Injury
    Date Received
    April 15, 2024
    Date of Event
    October 10, 2023
    Report Date
    April 15, 2024
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION
    Product Code
    LGW
    UDI-DI
    08714729767725
    PMA / PMN Number
    P030017
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    ADDITIONAL SUSPECT MEDICAL DEVICE COMPONENT INVOLVED IN THE EVENT: PRODUCT FAMILY: SCS-LINEAR LEADS UPN: M365SC2218500 MODEL: SC-2218-50 SERIAL: (B)(6) BATCH: 7132141.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PATIENTS ORIGINAL LEAD PLACEMENT WAS NOT COVERING THE CORRECT PAIN AREAS AND WAS CAUSING THORACIC AND ABDOMINAL STIMULATION DESPITE MULTIPLE REPROGRAMMING. THE PATIENT UNDERWENT A REVISION PROCEDURE WHEREIN THE LEADS WERE PULLED DOWN. THE PATIENT WAS DOING WELL POSTOPERATIVELY AND THE LEADS REMAIN IMPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1469472 LINEAR ST STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW BOSTON SCIENTIFIC NEUROMODULATION SC-2218-50 7130967 08714729767725

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR Female Required Intervention