BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INFINION 16

    MDR report key: 16856108 · Received May 2, 2023

    Report

    Report Number
    3006630150-2023-02434
    Event Type
    Injury
    Date Received
    May 2, 2023
    Date of Event
    April 12, 2023
    Report Date
    May 2, 2023
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION
    Product Code
    LGW
    UDI-DI
    08714729797807
    PMA / PMN Number
    P030017
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, 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: M365SC231650E0, MODEL: SC-2316-50E, SERIAL: (B)(6), BATCH: 7193518.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN AND NUMBNESS IN THE RIGHT LEG DURING THE TRIAL PERIOD. THE PATIENT UNDERWENT AN EARLY LEAD PULL PROCEDURE. NO DEVICE MALFUNCTION WAS SUSPECTED. THE EXPLANTED TRIAL LEADS WERE DISCARDED BY THE FACILITY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    123780 INFINION 16 STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW BOSTON SCIENTIFIC NEUROMODULATION SC-2316-50E 7192613 08714729797807

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Male Required Intervention