BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LP10 VOLUME VENTILATOR

    MDR report key: 70199 · Received February 13, 1997

    Report

    Report Number
    2183157-1997-00044
    Event Type
    Malfunction
    Date Received
    February 13, 1997
    Date of Event
    January 14, 1997
    Report Date
    January 14, 1997
    Manufacturer
    AEQUITRON MEDICAL, INC.
    Product Code
    CBK
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    DURING SERVICE OF PRODUCT UNIT WAS FOUND TO NOT CYCLE, WITH ALL LEDS AND CONSTANT SINGLE TONE ALARM, DUE TO INTEGRATED CIRCUIT U28 ON THE LOGIC BOARD BEING OUT OF SPEC. REPLACED U28.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LP10 VOLUME VENTILATOR VOLUME VENTILATOR CBK AEQUITRON MEDICAL, INC. LP10 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other