BEUDAMED
    FDA Adverse Event Death Summary report: N

    QUINTON CATHETER

    MDR report key: 111593 · Received July 31, 1997

    Report

    Report Number
    MW1011854
    Event Type
    Death
    Date Received
    July 31, 1997
    Manufacturer
    QUINTON INSTRUMENT CO.
    Product Code
    MSD
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PT EXSANQUINATED FROM QUINTON CATH. (CAP CAME APART FROM CATHETER) AT HOME. CATHETER USED FOR HEMODIALYZER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUINTON CATHETER Implant * MSD QUINTON INSTRUMENT CO. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death