BEUDAMED
    FDA Adverse Event Other Summary report: N

    SPINAL CORD STIMULATO

    MDR report key: 17383326 · Received July 21, 2023

    Report

    Report Number
    MW5119938
    Event Type
    Other
    Date Received
    July 21, 2023
    Report Date
    July 19, 2023
    Manufacturer
    ABBOTT MEDICAL
    Product Code
    LGW
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    DESCRIPTION OF EVENT: CALLER STATED THEY'RE PURSUING THE MDT PUMP BECAUSE THEIR ABBOTT SCS 'ISN'T WORKING. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    470488 SPINAL CORD STIMULATO STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW ABBOTT MEDICAL

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown