BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    840 VENTILATOR

    MDR report key: 2002374 · Received January 27, 2011

    Report

    Report Number
    8020893-2011-00039
    Event Type
    Malfunction
    Date Received
    January 27, 2011
    Date of Event
    December 30, 2010
    Report Date
    December 30, 2010
    Manufacturer
    PURITAN BENNETT CORP
    Product Code
    CBK
    PMA / PMN Number
    K970460
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    NPB HAS ATTEMPTED TO CONTACT CUSTOMER IN REGARDS TO EVENT. NO CUSTOMER RESPONSE. NPB WILL NOTIFY FDA SHOULD FURTHER INFO BECOME AVAILABLE.

    Description of Event or Problem · 1

    THE SERVICE REPORT SHOWS THE CUSTOMER REPORTED THAT THE 840 VENTILATOR STOPPED CYCLING WHILE IN USE ON A PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 840 VENTILATOR VENTILATOR CBK PURITAN BENNETT CORP 840

    Patients

    Seq Age Sex Outcome Treatment
    1