BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    840 VENTILATOR

    MDR report key: 1041243 · Received May 9, 2008

    Report

    Report Number
    8020893-2008-00219
    Event Type
    Malfunction
    Date Received
    May 9, 2008
    Date of Event
    May 7, 2008
    Report Date
    May 7, 2008
    Manufacturer
    PURITAN-BENNETT CORP.
    Product Code
    CBK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE 840 VENTILATOR STOPPED CYCLING WHILE IN USE ON A PATIENT. THE PATIENT WAS NOT HARMED OR INJURED AS A RESULT OF THE EVENT. THE PURITAN BENNETT (CSE) WAS NOT AUTHORIZED TO REPAIR THE VENTILATOR. THE HOSPITAL BIOMED WAS UNABLE TO DUPLICATE THE ALLEGED COMPLAINT. AS PER HOSPITAL BIOMED THE VENTILATOR TESTED ACCORDING TO THEIR SPECS.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1