BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INFINION 16

    MDR report key: 16458472 · Received March 1, 2023

    Report

    Report Number
    3006630150-2023-00938
    Event Type
    Injury
    Date Received
    March 1, 2023
    Date of Event
    February 5, 2023
    Report Date
    March 21, 2023
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION
    Product Code
    LGW
    UDI-DI
    08714729797807
    PMA / PMN Number
    P030017
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, 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)(4), BATCH: 7191582.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PATIENT HAD A SUSPECTED EPIDURAL HEMATOMA FROM THE TRIAL PROCEDURE. THE PATIENT UNDERWENT AN EARLY LEAD PULL PROCEDURE.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PATIENT HAD A SUSPECTED EPIDURAL HEMATOMA FROM THE TRIAL PROCEDURE. THE PATIENT UNDERWENT AN EARLY LEAD PULL PROCEDURE. ADDITIONAL INFORMATION WAS RECEIVED THAT THE PHYSICIAN DID NOT THINK THAT IT WAS HEMATOMA BUT HAD TO RULE IT OUT. THE EXPLANTED TRIAL LEADS WERE NOT RETURNED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1292315 INFINION 16 STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW BOSTON SCIENTIFIC NEUROMODULATION SC-2316-50E 7191283 08714729797807

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Female Required Intervention