BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SERVO-I

    MDR report key: 1231764 · Received August 19, 2008

    Report

    Report Number
    1225700-2008-00142
    Event Type
    Malfunction
    Date Received
    August 19, 2008
    Date of Event
    July 16, 2008
    Report Date
    July 22, 2008
    Manufacturer
    MAQUET CRITICAL CARE AB
    Product Code
    CBK
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    IT IS REPORTED THAT THE VENTILATOR GENERATED HIGH PRESSURE ALARMS AFTER FIVE DAYS OF BEING CONNECTED TO A PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SERVO-I CBK CBK MAQUET CRITICAL CARE AB * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *