BEUDAMED
    FDA Adverse Event Other Summary report: N

    CENTRAL VENOUS CATHETER

    MDR report key: 212360 · Received March 2, 1999

    Report

    Report Number
    1056436-1999-00031
    Event Type
    Other
    Date Received
    March 2, 1999
    Date of Event
    December 24, 1998
    Manufacturer
    NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.
    Product Code
    LJT
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US

    Narratives

    Description of Event or Problem · 1

    ON 02/01/1999, THE MFR REC'D A MEDWATCH REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRAL VENOUS CATHETER CHRONIC SILICONE CATHETER LJT NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Other