BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    MDR report key: 16118677 · Received January 6, 2023

    Report

    Report Number
    3014704491-2022-00731
    Event Type
    Malfunction
    Date Received
    January 6, 2023
    Date of Event
    November 19, 2022
    Report Date
    January 17, 2023
    Manufacturer
    BD (SUZHOU)
    Product Code
    FOZ
    PMA / PMN Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CH
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    A DEVICE EVALUATION IS ANTICIPATED BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

    Additional Manufacturer Narrative · 0

    H6: INVESTIGATION SUMMARY: A DEVICE HISTORY REVIEW WAS CONDUCTED FOR LOT NUMBER 2082612. 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. A SAMPLE COULD NOT BE OBTAINED FOR EVALUATION AND TESTING; IN LIEU OF THE AFFECTED DEVICE, VISUAL ANALYSIS WAS PERFORMED ON RETENTION SAMPLES FOR THIS LOT, THE RETAINED DEVICES WERE FOUND TO BE FREE OF ANY DAMAGE OR OTHER ABNORMALITIES. UNFORTUNATELY 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 · 0

    IT WAS REPORTED THAT THE END CAP OF THE BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM WAS DISCOLORED TO YELLOW. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE: "INTRAVENOUS INFUSION WAS PERFORMED. THE NURSE OPENED THE INDWELLING NEEDLE PACKAGE AND FOUND THAT THE PRN WAS YELLOW AND OXIDIZED. THE INDWELLING NEEDLE WAS REPLACED IMMEDIATELY, AND NO ADVERSE CONSEQUENCES WERE CAUSED."

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE END CAP OF THE BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM WAS DISCOLORED TO YELLOW. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE: "INTRAVENOUS INFUSION WAS PERFORMED. THE NURSE OPENED THE INDWELLING NEEDLE PACKAGE AND FOUND THAT THE PRN WAS YELLOW AND OXIDIZED. THE INDWELLING NEEDLE WAS REPLACED IMMEDIATELY, AND NO ADVERSE CONSEQUENCES WERE CAUSED."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1535948 BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM INTRAVASCULAR CATHETER FOZ BD (SUZHOU) 2082612

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown