BEUDAMED
    FDA Adverse Event Injury Summary report: N

    REDITUBE

    MDR report key: 5488412 · Received March 9, 2016

    Report

    Report Number
    5488412
    Event Type
    Injury
    Date Received
    March 9, 2016
    Date of Event
    December 18, 2015
    Report Date
    January 3, 2016
    Manufacturer
    CAREFUSION 211, INC. DBA CAREFUSION
    Product Code
    CBI
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE PATIENT WAS EXTUBATED WITH THE CUFF STILL INFLATED - EVEN WITH PILOT DEFLATED. WE THEN CUT PILOT LINE - THE CUFF STILL WOULD NOT DEFLATE PER THE CRNA REPORTING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    145495 REDITUBE TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR) CBI CAREFUSION 211, INC. DBA CAREFUSION

    Patients

    Seq Age Sex Outcome Treatment
    1