BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD INTIMA-II CATHETER Y 20GAX1.16 IN

    MDR report key: 8646338 · Received May 28, 2019

    Report

    Report Number
    3006948883-2019-00407
    Event Type
    Malfunction
    Date Received
    May 28, 2019
    Date of Event
    April 29, 2019
    Report Date
    June 28, 2019
    Manufacturer
    BD (SUZHOU)
    Product Code
    FOZ
    PMA / PMN Number
    K143610
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CH
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 0

    INVESTIGATION: A DEVICE HISTORY REVIEW WAS CONDUCTED FOR LOT NUMBER 6172128. 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. 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 NEEDLE HUB BROKEN DURING USE WITH A BD INTIMA-II CATHETER Y 20GAX1.16 IN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: IT WAS FOUND THE HANDLE OF NEEDLE HUB BROKEN DURING PUNCTURE.

    Additional Manufacturer Narrative · 1

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

    Description of Event or Problem · 1

    IT WAS REPORTED THAT NEEDLE HUB BROKEN DURING USE WITH A BD INTIMA-II CATHETER Y 20GAX1.16 IN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM (B)(6) TO ENGLISH: IT WAS FOUND THE HANDLE OF NEEDLE HUB BROKEN DURING PUNCTURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    438049 BD INTIMA-II CATHETER Y 20GAX1.16 IN INTRAVASCULAR CATHETER FOZ BD (SUZHOU) 6172128

    Patients

    Seq Age Sex Outcome Treatment
    1 Other