BEUDAMED
    FDA Adverse Event Death Summary report: N

    ABBOTT

    MDR report key: 9558458 · Received December 30, 2019

    Report

    Report Number
    9558458
    Event Type
    Death
    Date Received
    December 30, 2019
    Date of Event
    December 18, 2019
    Report Date
    December 23, 2019
    Manufacturer
    ABBOTT
    Product Code
    DSQ
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    SC, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    VAD COORDINATOR NOTIFIED 12/17/2019 THAT PT WOULD BE TRANSITIONING TO HOSPICE CARE FROM SPINAL REHAB CENTER IN (B)(6). VAD COORDINATOR RECEIVED PHONE CALL 12/18/2019 THAT PT HAD EXPIRED AND GIVEN INSTRUCTIONS TO TURN OFF LVAD. NO FURTHER INFO RECEIVED FROM (B)(6) FACILITY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1323566 ABBOTT HEARTMATE II LVAS DSQ ABBOTT

    Patients

    Seq Age Sex Outcome Treatment
    1 79 YR Death