BEUDAMED
    FDA Adverse Event Other Summary report: N

    V-CATH

    MDR report key: 501765 · Received November 18, 2003

    Report

    Report Number
    2925153-2003-00012
    Event Type
    Other
    Date Received
    November 18, 2003
    Date of Event
    October 9, 2003
    Report Date
    October 31, 2003
    Manufacturer
    HDC CORP.
    Product Code
    DQO
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    "FOLLOWING AN UNSUCCESSFUL INSERTION INTO THE VEIN, A SECTION OF THE CATHETER REMAINED IN THE PATIENT'S VEIN DURING REMOVAL."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 V-CATH PICC CATHETER DQO HDC CORP. 350-75 1015

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention