BEUDAMED
    FDA Adverse Event Death Summary report: N

    VPAP S SUB-ASSY-AMERICAS

    MDR report key: 3924929 · Received July 1, 2014

    Report

    Report Number
    3007573469-2014-00005
    Event Type
    Death
    Date Received
    July 1, 2014
    Date of Event
    May 29, 2014
    Report Date
    July 1, 2014
    Manufacturer
    RESMED LTD
    Product Code
    BZD
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    OH, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    RESMED WAS INFORMED THAT A HOSPICE PT DIED SHORTLY AFTER BEING PLACED ON VPAP THERAPY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    381605 VPAP S SUB-ASSY-AMERICAS BZD RESMED LTD 2611902

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR Death OXYGEN CONCENTRATOR