BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AARON

    MDR report key: 271349 · Received March 27, 2000

    Report

    Report Number
    1030322-2000-00001
    Event Type
    Injury
    Date Received
    March 27, 2000
    Date of Event
    March 15, 2000
    Report Date
    March 24, 2000
    Manufacturer
    AARON MEDICAL INDUSTRIES
    Product Code
    GEI
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    NE, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PATIENT HAD AN OXYGEN CANNULA TO THE NOSE. A DRAPE COVERED THE SURGICAL AREA NEAR THE OXYGEN. WHEN THE CAUTERY WAS TURNED ON, IT STARTED THE DRAPE ON FIRE GIVING THE PATIENT FIRST AND SECOND DEGREE BURNS TO THE NOSE AND EAR. THE FIRE WAS PUT OUT WITHOUT FURTHER INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AARON CAUTERY GEI AARON MEDICAL INDUSTRIES NA 0999A

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention