BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STERI-GAS 4-100 CARTRIDGE

    MDR report key: 259935 · Received January 21, 2000

    Report

    Report Number
    2110898-2000-00003
    Event Type
    Malfunction
    Date Received
    January 21, 2000
    Date of Event
    December 7, 1999
    Report Date
    January 12, 2000
    Manufacturer
    3M CO.
    Product Code
    FLI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A HEALTH CARE WORKER OPENED THE DOOR OF THE STERILIZER AND HAD A HARD TIME GETTING THE CARTRIDGE OUT. WORKER SAW LIQUID IN THE STERILIZER AND SOME LIQUID SPILLED ON HER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STERI-GAS 4-100 CARTRIDGE EO GAS CARTRIDGE FLI 3M CO. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR Other