BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INFINION 16

    MDR report key: 18909674 · Received March 14, 2024

    Report

    Report Number
    3006630150-2024-01483
    Event Type
    Injury
    Date Received
    March 14, 2024
    Date of Event
    February 22, 2024
    Report Date
    March 14, 2024
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION
    Product Code
    LGW
    UDI-DI
    08714729797807
    PMA / PMN Number
    P030017
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    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: 7230884.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PATIENT WAS SENT TO EMERGENCY DEPARTMENT FOR PAIN MEDICATION DUE TO PROCEDURAL PAIN. IMAGING WAS DONE AND NO ISSUES WERE FOUND.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    755641 INFINION 16 STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW BOSTON SCIENTIFIC NEUROMODULATION SC-2316-50E 7230268 08714729797807

    Patients

    Seq Age Sex Outcome Treatment
    1 71 YR Female Other| H