BEUDAMED
    FDA Adverse Event Death Summary report: N

    RESPIRATORY BREATHING CIRCUIT

    MDR report key: 253554 · Received December 7, 1999

    Report

    Report Number
    1718887-1999-00005
    Event Type
    Death
    Date Received
    December 7, 1999
    Report Date
    November 30, 1999
    Manufacturer
    MARQUEST MEDICAL PRODUCTS, INC.
    Product Code
    BZO
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A NURSE MAYBE CHANGED EXHALATION DRIVE LINE AND INSPIRATORY SENSING LINE UNINTENTIONALLY. SHE INSIST EXHALATION DRIVE LINE IS CONNECTED WITH BACTERIA FILTER AND SHORT LINE WHICH IS USUALLY USED FOR PROXIMAL PRESSURE SENSING LINE. SHE SAID PROXIMAL PRESSURE SENSING LINE WAS JUST NORMAL. USER FACILITY HAD SUCH A CLAIM BEFORE, BUT FACILITY IS TO GET A OFFICIAL COMMENT ABOUT THIS. A PATIENT IS DEAD BECAUSE OF THIS MISTAKE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESPIRATORY BREATHING CIRCUIT RESPIRATORY BREATHING CIRCUIT BZO MARQUEST MEDICAL PRODUCTS, INC. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death