BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    MDR report key: 12846492 · Received November 19, 2021

    Report

    Report Number
    3014704491-2021-00283
    Event Type
    Malfunction
    Date Received
    November 19, 2021
    Date of Event
    September 1, 2021
    Report Date
    November 22, 2021
    Manufacturer
    BECTON DICKINSON MEDICAL DEVICES CO., LTD. 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

    H.6. INVESTIGATION: A DEVICE HISTORY REVIEW WAS CONDUCTED FOR LOT NUMBER 1051525. 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, FUNCTIONAL TESTING WAS PERFORMED ON RETENTION SAMPLES FOR THIS LOT, THE RESULTS OF THESE SHOW THAT THE TESTED UNITS PERFORMED WITHIN PRODUCT SPECIFICATIONS. UNFORTUNATELY WITHOUT THE ABILITY TO INVESTIGATE THE AFFECTED UNIT OUR QUALITY ENGINEERS WERE UNABLE TO DETERMINE THE ROOT CAUSE FOR THIS COMPLAINT.SEE H.10.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM EXPERIENCED PRN SWELLING DURING INFUSION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: ON (B)(6) 2021 PATIENTS HOSPITALIZED IN THE HOSPITAL FOR INFECTIOUS FEVER, GASTRITIS TREATMENT, THE NURSE FOUND IN NEEDLE PUNCHING TUBE PRN APPEARED BUBBLE, STOP USING IMMEDIATELY AND REPLACE THE SAME ORIGIN OF THE SAME BATCH NUMBER THE SAME TYPE OF CLOSED VENOUS INDWELLING NEEDLE, DID NOT CAUSE HARM TO PATIENTS, SUBSEQUENT OPERATIONS, THE SAME BATCH PRODUCTS, FOUND NO SIMILAR PROBLEMS.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM EXPERIENCED PRN SWELLING DURING INFUSION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: ON (B)(6) 2021 PATIENTS HOSPITALIZED IN THE HOSPITAL FOR INFECTIOUS FEVER, GASTRITIS TREATMENT, THE NURSE FOUND IN NEEDLE PUNCHING TUBE PRN APPEARED BUBBLE, STOP USING IMMEDIATELY AND REPLACE THE SAME ORIGIN OF THE SAME BATCH NUMBER THE SAME TYPE OF CLOSED VENOUS INDWELLING NEEDLE, DID NOT CAUSE HARM TO PATIENTS, SUBSEQUENT OPERATIONS, THE SAME BATCH PRODUCTS, FOUND NO SIMILAR PROBLEMS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1744934 BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM INTERVASCULAR CATHETER FOZ BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU 1051525

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown