BEUDAMED
    FDA Adverse Event Other Summary report: N

    AVECOR

    MDR report key: 42328 · Received September 30, 1996

    Report

    Report Number
    42328
    Event Type
    Other
    Date Received
    September 30, 1996
    Date of Event
    September 23, 1996
    Report Date
    September 26, 1996
    Manufacturer
    AVECOR
    Product Code
    DTZ
    Report Source
    User Facility report
    Reporter Location
    WA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    OXYGENATOR FIBER LEAK NOTED BEFORE CASE STARTED IN OR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AVECOR OXYGENATOR DTZ AVECOR * *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other