BEUDAMED
    FDA Adverse Event Death Summary report: N

    THORATECH LABORATORIES

    MDR report key: 64654 · Received January 23, 1997

    Report

    Report Number
    MW1010619
    Event Type
    Death
    Date Received
    January 23, 1997
    Date of Event
    January 17, 1996
    Report Date
    January 20, 1997
    Manufacturer
    THORATECH LABORATORIES
    Product Code
    DSQ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    ADDITIONAL INFO RECEIVED FROM MFR ON 05/12/1998: THORATEC LABORATORIES CORP. HAS BEEN MISTAKENLY IDENTIFIED AS THE DEVICE MFR IN THE REFERENCED MEDWATCH REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 THORATECH LABORATORIES Implant VAD/VENTRICULAR ASSIST DEVICE DSQ THORATECH LABORATORIES * *

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR Death| H