BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    AUTOSOFT 90

    MDR report key: 19737517 · Received July 14, 2024

    Report

    Report Number
    3003442380-2024-14509
    Event Type
    Malfunction
    Date Received
    July 14, 2024
    Date of Event
    June 4, 2024
    Report Date
    July 14, 2024
    Manufacturer
    UNOMEDICAL A/S
    Product Code
    FPA
    UDI-DI
    05705244018150
    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 1913027- MDR 3003442380-2024-14509- DEVICE 1 OF 10.

    Description of Event or Problem · 0

    UNOMEDICAL REFERENCE NUMBER 1913027 EVENT OCCURRED IN THE UNITED STATES. ON 04-JUNE-2024, IT WAS REPORTED BY THE PATIENT THAT TEN INFUSION SET CANNULA WAS KINKED AFTER 3 HOURS OF USE. INFUSION SET WAS PLACED IN LOWER BACK. PATIENT REPLACED 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 WAS AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    209925 AUTOSOFT 90 UNO INSET II 110/6 GREY TCAP 10PK INT FPA UNOMEDICAL A/S 1002818 UNKNOWN 05705244018150

    Patients

    Seq Age Sex Outcome Treatment
    1 22 YR Male