BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LP10 VOLUME VENTILATOR

    MDR report key: 217575 · Received March 29, 1999

    Report

    Report Number
    2183157-1999-00076
    Event Type
    Malfunction
    Date Received
    March 29, 1999
    Date of Event
    March 8, 1999
    Report Date
    March 26, 1999
    Manufacturer
    NELLCOR PURITAN BENNETT
    Product Code
    CBK
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING SERVICE THE UNIT WAS FOUND NOT TO CYCLE WITH ALL LIGHT EMITTING DIODES ON AND CONSTANT SINGLE TONE ALARM DUE TO INTEGRATED CIRCUIT U28 ON THE LOGIC BOARD NOT BEING SEATED PROPERLY. RESEATED U28.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LP10 VOLUME VENTILATOR VOLUME VENTILATOR CBK NELLCOR PURITAN BENNETT LP10 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other