BEUDAMED
    FDA Adverse Event Other Summary report: N

    MAHURKAR CATHETER KIT

    MDR report key: 418195 · Received September 23, 2002

    Report

    Report Number
    1317749-2002-00019
    Event Type
    Other
    Date Received
    September 23, 2002
    Date of Event
    August 30, 2002
    Report Date
    September 23, 2002
    Manufacturer
    TYCOHEALTHCARE/KENDALL
    Product Code
    LFJ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO TYCOHEALTHCARE/KENDALL ON 8/03/2002 THAT A CUSTOMER HAD A PROBLEM WITH A MAHURKER CATHETER KIT. ACCORDING TO THE CUSTOMER DURING INSPECTION, THE GUIDE WIRE REMAINED IN THE VESSEL. CUSTOMER STATES THAT THE PT HAD TO BE RUSHED TO THE HOSPITAL FOR IMMEDIATE ATTENTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MAHURKAR CATHETER KIT DIALYSIS CATHETER LFJ TYCOHEALTHCARE/KENDALL * *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other