BEUDAMED
    FDA Adverse Event Other Summary report: N

    VAPORIZER

    MDR report key: 25428 · Received September 12, 1995

    Report

    Report Number
    MW1006903
    Event Type
    Other
    Date Received
    September 12, 1995
    Date of Event
    August 23, 1995
    Report Date
    August 31, 1995
    Manufacturer
    OHMEDA, INC.
    Product Code
    BSZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CO, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PTS DEVELOPED PULMONARY EDEMA FOLLOWING ORTHOPEDIC PROCEDURES. BOTH PTS WERE IN THE SAME OR, HAD SAME ANESTHESIOLOGIST & SURGEON. EQUIPMENT USED WAS THE SAME FOR BOTH PTS.

    Description of Event or Problem · 1

    PTS DEVELOPED PULMONARY EDEMA FOLLOWING ORTHOPEDIC PROCEDURES. BOTH PTS WERE IN THE SAME OR, HAD SAME ANESTHESIOLOGIST & SURGEON. EQUIPMENT USED WAS THE SAME FOR BOTH PTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VAPORIZER VAPORIZER BSZ OHMEDA, INC. TEC 6

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other