BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDTRONIC MINIMED 780G INSULIN PUMP

    MDR report key: 24322405 · Received February 12, 2026

    Report

    Report Number
    MW5183718
    Event Type
    Injury
    Date Received
    February 12, 2026
    Date of Event
    February 6, 2026
    Report Date
    February 6, 2026
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    OZP
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    003
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I EXPERIENCED HYPERGLYCEMIA AT (B)(6) 2026 12:41P ET. I USE MEDTRONIC MINIMED 780G INSULIN PUMP & ABBOTT INSTINCT CGM SENSOR SIGNAL. NO ALARM SOUNDED. "SN: (B)(6)." PATIENT CODE: 1905. DEVICE: 1012, 3015. REF REPORT: MW5183719.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    390263 MEDTRONIC MINIMED 780G INSULIN PUMP AUTOMATED INSULIN DOSING DEVICE SYSTEM, SINGLE HORMONAL CONTROL OZP MEDTRONIC MINIMED MMT-1884

    Patients

    Seq Age Sex Outcome Treatment
    1 Female Other