BEUDAMED
    FDA Adverse Event Other Summary report: N

    TRILOGY

    MDR report key: 17978283 · Received October 19, 2023

    Report

    Report Number
    MW5147231
    Event Type
    Other
    Date Received
    October 19, 2023
    Date of Event
    February 15, 2017
    Report Date
    October 16, 2023
    Manufacturer
    PHILIPS/ RESPIRONICS INC.
    Product Code
    NOU
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    ID, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    MY MOM WAS ON THE CPAP /BIPAP BUT VENTILATOR SETTINGS, KEPT COMPLAINING OF HER MASK LEAKING OR NOT WORKING CORRECTLY, THERE WAS WHITE DUST PARTIALS THAT WOULD COME FROM THE MACHINE. SHE THEN SWITCHED MACHINES AND GOT WORSE WHICH ENDED IN DEATH. CAN GET ADDITIONAL INFORMATION FROM HOSPITAL. REFERENCE REPORT MW5147232.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    933134 TRILOGY CONTINUOUS, VENTILATOR, HOME USE NOU PHILIPS/ RESPIRONICS INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR Female Disability| L| H| D| O AZITHROMYCIN| CALCIUM| LOSARTAN| NASAL SPRAY| PREDNISONE| PROBIOTICS