BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CATHETER

    MDR report key: 20246 · Received March 14, 1995

    Report

    Report Number
    MW1005426
    Event Type
    Injury
    Date Received
    March 14, 1995
    Date of Event
    February 15, 1995
    Report Date
    February 27, 1995
    Manufacturer
    VAS-CATH OF CANADA, LTD.
    Product Code
    LFK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    LA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    INFECTED 19 CM SOFT CELL CATHETER IN RIGHT GROIN WAS REMOVED AND REPLACED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CATHETER Implant CATHETER LFK VAS-CATH OF CANADA, LTD. 505-1859

    Patients

    Seq Age Sex Outcome Treatment
    1 88 YR Hospitalization| R