BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SERVO-I

    MDR report key: 3150019 · Received June 3, 2013

    Report

    Report Number
    3008355164-2013-00140
    Event Type
    Malfunction
    Date Received
    June 3, 2013
    Date of Event
    February 28, 2013
    Report Date
    May 28, 2013
    Manufacturer
    MAQUET CRITICAL CARE AB
    Product Code
    CBK
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    JA
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE VENTILATOR GENERATED A LOW EXPIRATORY MINUTE VOLUME ALARM. THERE WAS NO IMPACT ON PATIENT. (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    243181 SERVO-I CBK MAQUET CRITICAL CARE AB NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NI