BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AARON

    MDR report key: 222974 · Received May 10, 1999

    Report

    Report Number
    1030322-1999-00002
    Event Type
    Injury
    Date Received
    May 10, 1999
    Date of Event
    April 29, 1999
    Report Date
    May 6, 1999
    Manufacturer
    AARON MEDICAL INDUSTRIES
    Product Code
    GEI
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    DURING SURGICAL PROCEDURE A SUDDEN FLASH/FLAME OCCURRED, CAUSING THE EYEBROWS AND EYELASHES TO BE SINGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AARON CAUTERY GEI AARON MEDICAL INDUSTRIES NA 1098E

    Patients

    Seq Age Sex Outcome Treatment
    1 79 YR