BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LINEAR ST

    MDR report key: 11891382 · Received May 26, 2021

    Report

    Report Number
    3006630150-2021-02431
    Event Type
    Injury
    Date Received
    May 26, 2021
    Date of Event
    June 20, 2019
    Report Date
    May 26, 2021
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION
    Product Code
    LGW
    UDI-DI
    08714729767749
    PMA / PMN Number
    P030017
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    ADDITIONAL SUSPECT MEDICAL DEVICE COMPONENT INVOLVED IN THE EVENT: PRODUCT FAMILY: SCS-LINEAR LEADS, UPN: M365SC2218700, MODEL: SC-2218-70, SERIAL: (B)(4), BATCH: 5124022.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT PATIENT EXPERIENCED INADEQUATE PAIN RELIEF DESPITE REPROGRAMMING ATTEMPTS. X-RAY SHOWED THAT THE LEADS HAD MIGRATED. THE PATIENT UNDERWENT A REVISION PROCEDURE WHEREIN LEADS WERE ADDED AND THE EXISTING LEADS WERE REPOSITIONED. THE PATIENT WAS DOING WELL POSTOPERATIVELY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    787238 LINEAR ST STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW BOSTON SCIENTIFIC NEUROMODULATION SC-2218-70 5122087 08714729767749

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR Required Intervention