BEUDAMED
    FDA Adverse Event Other Summary report: N

    VERNITRON

    MDR report key: 286786 · Received July 25, 2000

    Report

    Report Number
    286786
    Event Type
    Other
    Date Received
    July 25, 2000
    Date of Event
    July 13, 2000
    Report Date
    July 25, 2000
    Manufacturer
    VERNITRON MEDICAL PRODUCTS
    Product Code
    FLE
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    NY, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    COVER BLEW OFF CAN OF BIOHAZARD WASTE WHEN BEING REMOVED FROM AUTOCLAVE AT THE COMPLETION OF CYCLE. WASTE WAS NON-INFECTIOUS. EMPLOYEE SUSTAINED BURNS TO FACE AND NECK. REQUIRED AND RECEIVED MEDICAL ATTENTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERNITRON STEAM STERILIZER FLE VERNITRON MEDICAL PRODUCTS VERNA-CLAVE UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 42 YR Other