BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD¿ NEXIVA

    MDR report key: 8233023 · Received January 10, 2019

    Report

    Report Number
    1710034-2018-00998
    Event Type
    Malfunction
    Date Received
    January 10, 2019
    Date of Event
    December 1, 2018
    Report Date
    February 14, 2019
    Manufacturer
    BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.
    Product Code
    FOZ
    UDI-DI
    30382903835196
    PMA / PMN Number
    K102520
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 0

    CORRECTION: B.3. DATE OF EVENT: (B)(6) 2018. H.6. INVESTIGATION SUMMARY: ONE PHOTO WAS PROVIDED FOR EVALUATION OF THIS INCIDENT. PHOTO WAS OF A REPRESENTATIVE UNIT, WHICH CONSISTED OF THE CATHETER/ADAPTER AND EXTENSION LINE ASSEMBLIES. THERE WAS ALSO A TOP WEB OF A PACKAGE FROM AN 18GA BD NEXIVA CLOSED IV CATHETER SYSTEM S/P FROM LOT 8232654. ALTHOUGH THE PHOTO DID NOT REVEAL THE ACTUAL DEFECT; THERE IS WRITING ¿BREAKING POINT¿ AND AN ARROW POINTING TO THE LOCATION WHERE THE EXTENSION TUBING IS ADHERED WITHIN THE CLEAR PORT OF THE WINGED ADAPTER (STABILIZATION PLATFORM). THE PHOTO DOES NOT PROVIDE SUFFICIENT EVIDENCE TO IDENTIFY THE DEFECT OR TO ESTABLISH A ROOT CASE. DHR REVIEW FOR LOT 8232354; WAS PREVIOUSLY CONDUCTED FOR INVESTIGATION (B)(4), WHICH DISCLOSED THE FOLLOWING: LOT NUMBER WAS BUILT / PACKAGE ON NFA LINE 1 FROM 23AUG2018 THRU 26AUG2018 FOR THE AMOUNT OF (B)(4) EACH. ALL CHALLENGE, SET UP AND IN-PROCESS SAMPLES WERE PERFORMED PER SPECIFICATIONS. RELATIONSHIP OF DEVICE TO THE REPORTED INCIDENT: THE DEFECT WAS NOT CONFIRMED AND A DEFINITE ROOT CAUSE COULD NOT BE IDENTIFIED FOR THIS INCIDENT SINCE NO SAMPLE WAS RETURNED. HOWEVER, THE DEFECT DESCRIBED IN THE PHOTO IS A KNOWN ISSUE AND THE MOST LIKELY ROOT CAUSE WAS THE MANUFACTURING PROCESS. MANUFACTURING: THE DEFECT IDENTIFIED IN THIS INCIDENT WAS CREATED AT THE ZONE 8 ADHESIVE DISPENSE STATION AFTER THE STATION REDESIGN. IF AIR GOT IN THE LINES THAT FED ADHESIVE TO THE ADHESIVE DISPENSE GRIPPERS, A SHORT SHOT OF ADHESIVE WOULD BE DISPENSED ONTO THE TUBE. A NEW STATION DESIGN WAS INSTALLED ON NFA1 ZONE 8 IN APRIL 2018 (PROTOCOL (B)(4)) THAT THE EXTENSION TUBE ADHESIVE DISPENSE STATIONS ARE PURGED ON A REGULAR BASIS AND CURRENT PROCESS CONTROLS INCLUDE ROUTINE LEAK TEST AND EXT. PULL TEST WELL AS A 100% ONLINE FLOW TESTER IN ZONE 8.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THERE WERE FOUR TO FIVE BREAK OF BD¿ NEXIVAS DURING USE WITHIN A FEW DAY.

    Additional Manufacturer Narrative · 1

    DATE OF EVENT: UNKNOWN. THE DATE RECEIVED BY MANUFACTURER HAS BEEN USED FOR THIS FIELD. 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 THERE WERE FOUR TO FIVE BREAK OF BD¿ NEXIVAS DURING USE WITHIN A FEW DAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    25438 BD¿ NEXIVA PERIPHERAL VASCULAR CATHETER FOZ BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. 8232654 30382903835196

    Patients

    Seq Age Sex Outcome Treatment
    1 Other