BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LP10 VOLUME VENTILATOR

    MDR report key: 191472 · Received October 8, 1998

    Report

    Report Number
    2183157-1998-00172
    Event Type
    Malfunction
    Date Received
    October 8, 1998
    Date of Event
    September 8, 1998
    Manufacturer
    NELLCOR PURITAN BENNETT
    Product Code
    CBK
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    NELLCOR PURITAN BENNETT REC'D A CALL FROM A BIOMED TECH AT A FACILITY ON 09/08/1998. BIOMED TECH CALLED TO REPORT THE FOLLOWING PROBLEM: NO AUDIBLE ALARM.

    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 UNKNOWN Other