BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD INTIMA-II 22GAX0.75IN PRN SLM NPVC

    MDR report key: 16040151 · Received December 22, 2022

    Report

    Report Number
    3014704491-2022-00703
    Event Type
    Malfunction
    Date Received
    December 22, 2022
    Date of Event
    August 5, 2022
    Report Date
    January 15, 2023
    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 AND/OR DEVICE HISTORY REVIEW IS ANTICIPATED BUT IS NOT COMPLETE. UPON COMPLETION, A SUPPLEMENTAL REPORT WILL BE FILED.

    Additional Manufacturer Narrative · 0

    H6: INVESTIGATION SUMMARY: A DEVICE HISTORY REVIEW WAS CONDUCTED FOR LOT NUMBER 2110032. 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.

    Description of Event or Problem · 0

    IT WAS REPORTED WHILE USING BD INTIMA-II 22GAX0.75IN PRN SLM NPVC THE CLAMP DID NOT CLAMP. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS FOUND THAT THE INDWELLING NEEDLE STILL HAD BLOOD REFLUX AND THE SWITCH WAS TURNED OFF. IN THE STATE OF BLOOD FLOW BACK TO THE ENTIRE INDWELLING NEEDLE, IMMEDIATELY PULL OUT THE INDWELLING NEEDLE AND RE-INDWELL THE NEEDLE.

    Description of Event or Problem · 0

    IT WAS REPORTED WHILE USING BD INTIMA-II 22GAX0.75IN PRN SLM NPVC THE CLAMP DID NOT CLAMP. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: IT WAS FOUND THAT THE INDWELLING NEEDLE STILL HAD BLOOD REFLUX AND THE SWITCH WAS TURNED OFF. IN THE STATE OF BLOOD FLOW BACK TO THE ENTIRE INDWELLING NEEDLE, IMMEDIATELY PULL OUT THE INDWELLING NEEDLE AND RE-INDWELL THE NEEDLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2748214 BD INTIMA-II 22GAX0.75IN PRN SLM NPVC INTRAVASCUALR CATHETER FOZ BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU 2110032

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown