BEUDAMED
    FDA Adverse Event Other Summary report: N

    HOWES MULTI-LUMEN CENTRAL VENOUS CATHETERIZATION KIT, 7 FR.

    MDR report key: 18213 · Received December 5, 1994

    Report

    Report Number
    MW1004311
    Event Type
    Other
    Date Received
    December 5, 1994
    Date of Event
    October 12, 1994
    Report Date
    November 4, 1994
    Manufacturer
    ARROW INTERNATIONAL, INC.
    Product Code
    DQO
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    A 20 GUAGE NEEDLE WOULD NOT ACCOMODATE GUIDE WIRE FOR CVP INSERTION. ALL ITEMS USED WERE PART OF THE SAME TRIPLE LUMEN KIT. ANOTHER CVP KIT WAS SUCCESSFUL FOR INSERTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HOWES MULTI-LUMEN CENTRAL VENOUS CATHETERIZATION KIT, 7 FR. Implant DQO ARROW INTERNATIONAL, INC. AK-15703-B AK-1-175-4

    Patients

    Seq Age Sex Outcome Treatment
    1 44 YR Other