BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    AUTOSOFT XC

    MDR report key: 19475476 · Received June 6, 2024

    Report

    Report Number
    3003442380-2024-06642
    Event Type
    Malfunction
    Date Received
    June 6, 2024
    Date of Event
    January 28, 2024
    Report Date
    June 6, 2024
    Manufacturer
    UNOMEDICAL A/S
    Product Code
    FPA
    UDI-DI
    05705244016620
    PMA / PMN Number
    K032854
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    INITIAL AND FINAL MDR 1880801 - MDR 3003442380-2024-06642 - DEVICE 12 OF 15. (B)(6).

    Description of Event or Problem · 0

    UNOMEDICAL REFERENCE NUMBER (B)(4). EVENT OCCURRED IN THE UNITED STATES. IT WAS REPORTED THAT PATIENT FACED FIFTEEN INFUSION SET CANNULA KINKED EVENTS SINCE (B)(6) 2024. ALL THE EVENTS OCCURRED AFTER 3 HOURS OF INSERTION AND THE INSERTION SITE WAS AT ABDOMEN. ALL THE SET WERE IN USE FOR 4 TO 5 HOURS RESPECTIVELY. THE BLOOD GLUCOSE LEVEL AT THE TIME OF EVENT WAS 200 TO 300 MG/DL AND THE PATIENT RESOLVED IT BY CHANGING SOFT CANNULA INFUSION SET AND RESUMED INSULIN SUCCESSFULLY. UNOMEDICAL DO NOT SEE BENT/KINKING AS BEING RELATED TO HUMAN FACTORS, BUT RATHER AS A TRAINING ISSUE INCLUDING CORRECT CHOICES OF INSERTION SITES AND INFUSION SETS AND CANNULA LENGTH. FURTHERMORE, THE SOFT CANNULA IS A FLEXIBLE MATERIAL THAT DURING USE AND UPON REMOVAL CAN BEND SLIGHTLY. NO FURTHER INFORMATION AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1861861 AUTOSOFT XC UNO INSET I 60/6 GREY TCAP 10PK INT FPA UNOMEDICAL A/S 1001680 UNKNOWN 05705244016620

    Patients

    Seq Age Sex Outcome Treatment
    1 7 YR Female