BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CARDINAL AIRLIFE

    MDR report key: 3068033 · Received March 29, 2013

    Report

    Report Number
    3068033
    Event Type
    Malfunction
    Date Received
    March 29, 2013
    Date of Event
    March 28, 2013
    Report Date
    March 29, 2013
    Manufacturer
    CAREFUSION 211, INC.. DBA CAREFUSION
    Product Code
    CAT
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    FL, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PRODUCT IS STICKY.WHAT WAS THE ORIGINAL INTENDED PROCEDURE?O2 THERAPY.DEVICE #1IS THIS A LABORATORY DEVICE OR LABORATORY TEST?NO.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    131270 CARDINAL AIRLIFE CANNULA, NASAL, OXYGEN CAT CAREFUSION 211, INC.. DBA CAREFUSION * Y07E0070

    Patients

    Seq Age Sex Outcome Treatment
    1 *