BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    MDR report key: 9812983 · Received March 10, 2020

    Report

    Report Number
    3006948883-2020-00084
    Event Type
    Malfunction
    Date Received
    March 10, 2020
    Date of Event
    February 16, 2020
    Report Date
    February 28, 2020
    Manufacturer
    BD (SUZHOU)
    Product Code
    FOZ
    PMA / PMN Number
    N/A
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CH
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION SUMMARY: IN RESPONSE TO THE EVENT REPORTED BY YOUR FACILITY A DEVICE HISTORY REVIEW WAS CONDUCTED FOR LOT NUMBER 9023843. OUR RECORDS SHOW THAT THIS IS THE ONLY INSTANCE OF THIS ISSUE OCCURRING IN THIS PRODUCTION BATCH. ACCORDING TO THE SAMPLING PLAN APPLIED FOR PRODUCT PERFORMANCE, THIS LOT WAS ACCEPTED AND RELEASED WITHOUT DEFECTS BEING NOTED DURING THE FINAL ASSEMBLY OR VISUAL INSPECTIONS. UNFORTUNATELY A SAMPLE COULD NOT BE OBTAINED FOR EVALUATION AND TESTING. INVESTIGATION CONCLUSION: BD WILL CONTINUE TO MONITOR THIS ISSUE. ROOT CAUSE DESCRIPTION: WITHOUT THE ABILITY TO INVESTIGATE THE AFFECTED UNIT OUR QUALITY ENGINEERS WERE UNABLE TO DETERMINE THE ROOT CAUSE FOR THIS COMPLAINT.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM NEEDLE DISENGAGEMENT WAS DIFFICULT. THIS WAS DISCOVERED BEFORE USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE CHILD WAS ADMITTED TO HOSPITAL DUE TO ACUTE BRONCHOPNEUMONIAS, AND WAS GIVEN INTRAVENOUS INFUSION AS ADVISED BY THE DOCTOR. DURING THE INDWELLING NEEDLE PUNCTURE, THE NURSE CHECKED THE INDWELLING NEEDLE BEFORE THE PUNCTURE, AND FOUND THAT IT WAS DIFFICULT TO SEPARATE THE SOFT TROCAR FROM THE NEEDLE CORE, SO THE INDWELLING NEEDLE WAS TIMELY REPLACED, AND NO HARM WAS CAUSED TO THE CHILD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    278407 BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM CATHETER FOZ BD (SUZHOU) 9023843

    Patients

    Seq Age Sex Outcome Treatment
    1 Other