BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LP6+ VOLUME VENTILATOR

    MDR report key: 177303 · Received July 1, 1998

    Report

    Report Number
    2183157-1998-00102
    Event Type
    Malfunction
    Date Received
    July 1, 1998
    Date of Event
    June 3, 1998
    Report Date
    July 1, 1998
    Manufacturer
    NELLCOR PURITAN BENNETT
    Product Code
    CBK
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    RESPIRATORY THERAPIST

    Narratives

    Description of Event or Problem · 1

    SOURCE CALLED NELLCOR PURITAN BENNETT ON 06/03/1998 TO REPORT THE FOLLOWING PROBLEM: LOW PRESSURE ALARM DOES NOT SOUND UPON CIRCUIT DISCONNECT. NO PT HARM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LP6+ VOLUME VENTILATOR VOLUME VENTILATOR CBK NELLCOR PURITAN BENNETT LP6+ NA

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other