BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ILET BIONIC PANCREAS

    MDR report key: 22994103 · Received September 8, 2025

    Report

    Report Number
    3019004087-2025-02298
    Event Type
    Malfunction
    Date Received
    September 8, 2025
    Date of Event
    August 8, 2025
    Report Date
    September 8, 2025
    Manufacturer
    BETA BIONICS, INC.
    Product Code
    QFG
    UDI-DI
    850050080015
    PMA / PMN Number
    K231485
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    AT THE TIME OF THIS REPORT THE ILET EVALUATION IS STILL IN PROGRESS. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN INVESTIGATION IS COMPLETED.

    Description of Event or Problem · 0

    ON (B)(6) 2025, THE USER¿S CAREGIVER REPORTED THAT THE ILET DEVICE SCREEN WAS CRACKED AFTER THE DEVICE STRUCK A TABLE. THE DEVICE WAS NO LONGER USABLE. BLOOD GLUCOSE WAS NOT AFFECTED. NO MEDICAL INTERVENTION WAS REQUIRED. A REPLACEMENT DEVICE WAS ARRANGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1915474 ILET BIONIC PANCREAS ALTERNATE CONTROLLER ENABLED INSULIN INFUSION PUMP QFG BETA BIONICS, INC. BB1001 850050080015

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown DEXCOM G7 CONTINUOUS GLUCOSE MONITOR.