BEUDAMED
    FDA Adverse Event Other Summary report: N

    ZYNEX

    MDR report key: 2577637 · Received May 8, 2012

    Report

    Report Number
    1723686-2012-00007
    Event Type
    Other
    Date Received
    May 8, 2012
    Date of Event
    April 18, 2012
    Report Date
    May 8, 2012
    Manufacturer
    ZYNEX MEDICAL, INC.
    Product Code
    GZJ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE PT USED NEOSPORIN ON THE BURNS AND DID NOT SEEK ANY MEDICAL ATTENTION.

    Description of Event or Problem · 1

    PT REPORTED THAT SHE RECEIVED 3 BURNS ON HER SKIN, LEFT SIDE OF THE BACK. THE BURNS TURNED TO BLISTERS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZYNEX TENS ELECTRICAL STIMULATOR GZJ ZYNEX MEDICAL, INC. NEXWAVE

    Patients

    Seq Age Sex Outcome Treatment
    1 Other