BEUDAMED
    FDA Adverse Event Other Summary report: N

    STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

    MDR report key: 22508445 · Received July 15, 2025

    Report

    Report Number
    MW5172666
    Event Type
    Other
    Date Received
    July 15, 2025
    Report Date
    July 14, 2025
    Manufacturer
    ABBOTT MEDICAL
    Product Code
    LGW
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    PATIENT
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    REPORTER CALLED TO SUBMIT A REPORT ABOUT HIS PAIN STIMULATOR DEVICE'S REMOTE ISSUE. HE SAID THE BATTERY IS ON ONE SIDE AND THE GENERATOR IS ON THE OTHER SIDE. HE SAID HE HAS THE PAIN STIMULATOR IMPLANTED AFTER HE HAD A LOWER BACK SURGERY. HE SAID THE STIMULATOR DEVICE'S REMOTE WILL NOT CHARGE. THE DISPLAY IS VERY DIM AND HARD TO READ. HE SAID THE DEVICE DOES ONLY COVER HIS NECK PAIN BUT DOES NOT COVER HIS BACK PAIN. HE THINKS THE DEVICE SHIFTED AFTER HE FELL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    151035 STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW ABBOTT MEDICAL

    Patients

    Seq Age Sex Outcome Treatment
    1 90 YR Male