BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NEVRO SENZA SPINAL CORD STIMULATOR SYSTER

    MDR report key: 24769606 · Received April 2, 2026

    Report

    Report Number
    MW5186338
    Event Type
    Injury
    Date Received
    April 2, 2026
    Date of Event
    February 9, 2024
    Report Date
    March 30, 2026
    Manufacturer
    NEVRO CORP./GLOBUS MEDICAL, INC.
    Product Code
    LGW
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NV, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    NEVRO SPINAL CORD STIMULATOR WAS IMPLANTED. AND SERVICED FOR ABOUT A YEAR (COMPANY SAYS IT SUPPORTS FOR THE LIFE OF THE PRODUCT - ABOUT 10 YEARS) I HAVE MADE NUMEROUS CALLS TO LOCAL TECH SUPPORT (B)(6) SINCE (B)(6) 2025 -ALL WERE UNANSWERED. ALL CALLS TO NEVRO CORPORATE AND GLOBUS CORPORATE - NEVRO OWNER - ALSO HAVE NOT BEEN ANSWERED. INSTEAD OF REDUCING PAIN, STIMULATOR CAUSES ADDITIONAL PAIN WHICH IN TURN CASES SERIOUS LACK OF SLEEP, NARCOLEPSY, DIFFICULTY WALKING, HEART PROBLEMS, ETC. IT APPEARS TO ME TO BE A SIMILAR CASE TO THE STIMWAVE CASE A FEW YEARS AGO. PLEASE LOOK INTO THIS AND GET ME HELP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    833134 NEVRO SENZA SPINAL CORD STIMULATOR SYSTER STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW NEVRO CORP./GLOBUS MEDICAL, INC. NIPG2500 891053

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Other| S| R