BEUDAMED
    FDA Adverse Event Other Summary report: N

    ARROW - HOWES

    MDR report key: 448128 · Received March 13, 2003

    Report

    Report Number
    448128
    Event Type
    Other
    Date Received
    March 13, 2003
    Date of Event
    February 28, 2003
    Report Date
    March 12, 2003
    Manufacturer
    ARROW INTERNATIONAL, INC
    Product Code
    DQO
    Report Source
    User Facility report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    SURGEON WAS ATTEMPTING TO PLACE A CENTRAL VENOUS CATHETER, BUT WAS UNABLE TO THREAD THE GUIDEWIRE - IT DID NOT FIT THRU THE INTRODUCER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ARROW - HOWES MULTILUMEN CENTRAL VENOUS CATHETER KIT DQO ARROW INTERNATIONAL, INC AK-15703-B RF2100336

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR Other