BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CORTRAK 2 NASOGASTRIC/NASOINTESTINAL FEEDING TUBE WITH ELECTROMAGNETIC TRANSMIT

    MDR report key: 11499904 · Received March 16, 2021

    Report

    Report Number
    9611594-2021-00042
    Event Type
    Malfunction
    Date Received
    March 16, 2021
    Date of Event
    February 17, 2021
    Report Date
    April 30, 2021
    Manufacturer
    AVANOS MEDICAL INC.
    Product Code
    KNT
    UDI-DI
    00350770458021
    PMA / PMN Number
    K821906
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 0

    THE SAMPLE PROVIDED WAS EVALUATED CONFIRMING TUBING EXHIBITED BALLOONING. THE ROOT CAUSE OF THE REPORTED ISSUE COULD NOT BEEN CONCLUSIVELY DETERMINED. ALL INFORMATION REASONABLY KNOWN AS OF 29-APR-2021 HAS BEEN INCLUDED IN THIS HEALTH AUTHORITY REPORT. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A FOLLOW-UP HEALTH AUTHORITY REPORT WILL BE PROVIDED. THE INFORMATION PROVIDED BY AVANOS MEDICAL, INC. REPRESENTS ALL OF THE KNOWN INFORMATION AT THIS TIME. DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT/REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO AVANOS MEDICAL, INC. AVANOS MEDICAL, INC. HAS NO INDEPENDENT KNOWLEDGE OF THE EVENT REPORTED BUT IS RELAYING THE INFORMATION THAT WAS PROVIDED BY THE USER FACILITY WHERE THE INCIDENT OCCURRED. THIS PRODUCT INCIDENT IS DOCUMENTED IN THE AVANOS MEDICAL, INC. COMPLAINT DATABASE AND IDENTIFIED AS COMPLAINT (B)(4). THIS INFORMATION IS SUBMITTED PURSUANT TO 21CFR803, IN COMPLIANCE WITH THE MEDICAL DEVICE REPORTING REQUIREMENT AND SHOULD NOT BE CONSIDERED TO BE AN ADMISSION THAT AN AVANOS MEDICAL, INC. PRODUCT IS DEFECTIVE OR CAUSED SERIOUS INJURY.

    Additional Manufacturer Narrative · 1

    THE PRODUCT INVOLVED IN THE REPORT HAS BEEN RETURNED AND IS BEING PROCESSED FOR EVALUATION. A REVIEW OF THE DEVICE HISTORY RECORD IS NOT POSSIBLE AS NO LOT NUMBER WAS PROVIDED. UPON COMPLETION OF THE SAMPLE EVALUATION AND THE INVESTIGATION; A FOLLOW-UP REPORT WILL BE FILED. ALL INFORMATION REASONABLY KNOWN AS OF 15-MAR 2021 HAS BEEN INCLUDED IN THIS HEALTH AUTHORITY REPORT. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A FOLLOW-UP HEALTH AUTHORITY REPORT WILL BE PROVIDED. AVANOS MEDICAL, INC. HAS NO INDEPENDENT KNOWLEDGE OF THE EVENT REPORTED BUT IS RELAYING THE INFORMATION THAT WAS PROVIDED BY THE USER FACILITY WHERE THE INCIDENT OCCURRED. THIS PRODUCT INCIDENT IS DOCUMENTED IN THE AVANOS MEDICAL, INC. COMPLAINT DATABASE AND IDENTIFIED AS COMPLAINT COMP(B)(4).

    Description of Event or Problem · 1

    AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWO DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWO DIFFERENT EVENTS. THIS IS THE FIRST OF TWO REPORTS. REFER TO 9611594-2021-00043 FOR THE SECOND EVENT. IT WAS REPORTED ON (B)(6) 2021 AT 1900, THE PATIENT WAS ADMITTED WITH DYSPNEA ON EXERTION AND LEG SWELLING. THE 'DOBHOFF' WAS PLACED FOR TUBE FEEDING (TF) ON (B)(6) 2021 AT 2000. THE PATIENT WAS NOTED TO HAVE SIGNIFICANT TF RESIDUALS. THE TF WAS HELD FOR 2 HOURS ON (B)(6) 2021 AT 2300. THE TF WAS RESTARTED ON (B)(6) 2021 AT 0115. CLOG ZAPPER WAS INFUSED INTO THE DIGESTIVE HEALTH TUBE (DHT). A WIRE WAS INSERTED DUE TO BLOCKAGE ON (B)(6) 2021. IN THE MORNING AN X-RAY WAS REVIEWED AND NOTED THAT THE TUBE MAY HAVE BEEN TRANSECTED ON (B)(6) 2021 IN THE AFTERNOON. THE X-RAY SHOWED THE RESECTED DHT IN THE PATIENT'S STOMACH ON (B)(6) 2021 AT 1700. AN EGD WAS PERFORMED AT THE PATIENT'S BEDSIDE AND THE 'DOBHOFF' FRAGMENTS WERE NOTED IN THE PATIENT'S STOMACH. THE CLINICIAN SUCCESSFULLY REMOVED THE BROKEN DEVICE FRAGMENTS. ADDITIONAL INFORMATION RECEIVED (B)(6) 2021 STATED IT WAS NOT CONFIRMED IF THE CLINICIANS WAITED THE RECOMMENDED 30-60 MINUTES ONCE THEY USED THE CLOG ZAPPER AND THEN REINSERTED THE STYLET TO DETERMINE PATENCY. FOR ALL CONTINUOUS FEEDS THEY DO NOT HAVE AN ALARM FOR INCREASING TF PRESSURE. THE ALARM GOES OFF FOR AN OCCLUSION, NO WARNING, ONLY WHEN THERE IS AN OCCLUSION IDENTIFIED. THE DEVICE BROKE AT THE 28-30 CM MARK. THERE WAS ALSO A "THINNING" OF THE TUBE BELOW THE BREAK POINT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    395878 CORTRAK 2 NASOGASTRIC/NASOINTESTINAL FEEDING TUBE WITH ELECTROMAGNETIC TRANSMIT DH CORTRAK DISPOSABLES KNT AVANOS MEDICAL INC. 20-9432TRAK2 UNKNOWN 00350770458021

    Patients

    Seq Age Sex Outcome Treatment
    1