BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD INSYTE AUTOG BC

    MDR report key: 20832334 · Received December 3, 2024

    Report

    Report Number
    1710034-2024-01416
    Event Type
    Malfunction
    Date Received
    December 3, 2024
    Date of Event
    September 30, 2024
    Report Date
    December 12, 2024
    Manufacturer
    BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.
    Product Code
    FOZ
    UDI-DI
    00382903825448
    PMA / PMN Number
    K201075
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UT, US
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    INVESTIGATION RESULTS: A DEVICE HISTORY RECORD REVIEW WAS COMPLETED BY OUR QUALITY ENGINEER TEAM FOR PROVIDED MATERIAL NUMBER 382544 AND LOT NUMBER 4141835. THE REVIEW DID NOT REVEAL ANY DETECTED ABNORMALITIES DURING THE PRODUCTION PROCESS THAT COULD HAVE CONTRIBUTED TO THIS DEFECT AND ALL QUALITY TESTS WERE FOUND TO BE WITHIN SPECIFICATION. AS A SAMPLE WAS UNAVAILABLE FOR RETURN, A THOROUGH SAMPLE INVESTIGATION COULD NOT BE COMPLETED. BASED ON THE INVESTIGATION RESULTS, AN EXACT CAUSE FOR THIS INCIDENT COULD NOT BE IDENTIFIED.

    Additional Manufacturer Narrative · 0

    H.3. A FOLLOW UP MDR WILL BE SUBMITTED IF ADDITIONAL INFORMATION, A DEVICE EVALUATION, OR A DEVICE HISTORY REVIEW IS COMPLETED.

    Description of Event or Problem · 0

    NO ADDITIONAL INFORMATION.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT BD INSYTE AUTOG BC BLOOD CONTROL FEATURE DID NOT WORK. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WHEN YOU PLACE THE INSYTE AUTOGUARD BC IV CATHETER, IT IS SUPPOSED TO LET YOU RETRACT THE NEEDLE AND THE HUB OF THE IV CATHETER IS SUPPOSED TO NOT LEAK UNLESS THE MEMBRANE IS PUNCTURED. AFTER RETRACTING THE NEEDLE, THESE IV CATHETERS HAVE BEEN LEAKING FROM THE HUB. NOTHING HAD BEEN PLACED INSIDE WHICH SHOULD HAVE MADE THEM LEAK. IT HAPPENED BEFORE ANY CONNECTORS WERE ATTACHED. NOT A MAJOR SAFETY ISSUE, BUT NOT WORKING PROPERLY. I HAVE USED 2 TODAY WITH SAME RESULT THEY WERE BOTH 18 GA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1544158 BD INSYTE AUTOG BC PERIPHERAL IV CATHETERS FOZ BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. 4141835 00382903825448

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown