BEUDAMED
    FDA Adverse Event Summary report: N

    KNIGHTSTAR 330

    MDR report key: 1062404 · Received June 18, 2008

    Report

    Report Number
    8020893-2008-00289
    Date Received
    June 18, 2008
    Date of Event
    June 6, 2008
    Report Date
    June 6, 2008
    Manufacturer
    NELLCOR PURITAN BENNETT
    Product Code
    CBK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    NELLCOR PURITAN BENNETT RECEIVED INFO STATING DEVICE STOP CYCLING DURING PT USE. NO PT INJURY REPORTED AND NO CHANGE IN THERAPY, DUE TO THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KNIGHTSTAR 330 BI-LEVEL VENTILATOR CBK NELLCOR PURITAN BENNETT KNIGHTSTAR 330

    Patients

    Seq Age Sex Outcome Treatment
    1