BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    KION

    MDR report key: 1222885 · Received August 15, 2008

    Report

    Report Number
    1225700-2008-00137
    Event Type
    Malfunction
    Date Received
    August 15, 2008
    Date of Event
    July 4, 2008
    Report Date
    August 4, 2008
    Manufacturer
    MAQUET CRITICAL CARE AB
    Product Code
    BSZ
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    SW
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    THE HOSP REPORTED THAT A WHEEL LOOSENED OFF THE ANESTHESIA MACHINE WHILE IT WAS BEING MOVED AND IT FELL. NO PT WAS CONNECTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KION BSZ BSZ MAQUET CRITICAL CARE AB * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *