BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRECISION SPECTRA

    MDR report key: 9748335 · Received February 24, 2020

    Report

    Report Number
    3006630150-2020-00766
    Event Type
    Injury
    Date Received
    February 24, 2020
    Date of Event
    October 16, 2019
    Report Date
    February 24, 2020
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION
    Product Code
    LGW
    UDI-DI
    08714729821526
    PMA / PMN Number
    P030017
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SD, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    MODEL NUMBER/ CATALOG NUMBER: SC-2218-50, SERIAL NUMBER: (B)(4), BATCH/ LOT NUMBER: 21086016 / 21160214, MODEL/ CATALOG DESCRIPTION: LINEAR ST LEAD KIT 50 CM. MODEL NUMBER/ CATALOG NUMBER: SC-2218-70, SERIAL NUMBER: (B)(4), BATCH/ LOT NUMBER: 5001599, MODEL/ CATALOG DESCRIPTION: LINEAR ST LEAD KIT 70 CM. THE EXPLANTED DEVICES WERE NOT RETURNED TO BSN AS THEY WERE DISCARDED BY THE MEDICAL FACILITY.

    Description of Event or Problem · 1

    A REPORT WAS RECEIVED THA THE PATIENT WAS EXPERIENCING OVERSTIMULATION AND INADEQUATE STIMULATION. THE PATIENT UNDERWENT AN EXPLANT PROCEDURE AND WAS DOING WELL POSTOPERATIVELY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    208770 PRECISION SPECTRA STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW BOSTON SCIENTIFIC NEUROMODULATION SC-1132 21118433 08714729821526

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR Required Intervention