BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TEC 6

    MDR report key: 2201197 · Received July 29, 2011

    Report

    Report Number
    2112667-2011-00039
    Event Type
    Malfunction
    Date Received
    July 29, 2011
    Date of Event
    March 14, 2011
    Report Date
    July 29, 2011
    Manufacturer
    DATEX-OHMEDA INC.
    Product Code
    CAD
    PMA / PMN Number
    K913593
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    THE HOSPITAL REPORTED THAT THE OUTPUT OF THEIR VAPORIZER WAS LOWER THAN EXPECTED. THERE WAS NO REPORT OF PT INVOLVEMENT. GE HEALTHCARE'S INVESTIGATION IS ONGOING. A F/U REPORT WILL BE SUBMITTED ONCE THE INVESTIGATION HAS BEEN COMPLETED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TEC 6 ANESTHESIA VAPORIZER CAD DATEX-OHMEDA INC.

    Patients

    Seq Age Sex Outcome Treatment
    1