BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INSULIN PUMP

    MDR report key: 22883944 · Received August 25, 2025

    Report

    Report Number
    MW5175177
    Event Type
    Malfunction
    Date Received
    August 25, 2025
    Date of Event
    May 1, 2025
    Report Date
    June 2, 2025
    Manufacturer
    MEDTRONIC MINIMED, INC.
    Product Code
    OZP
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    MEDTRONIC UPDATE: URGENT MEDICAL DEVICE CORRECTION. MINIMED 600 AND 700 SERIES PUMP SYSTEMS - BATTERY STATUS ALERTS AND ALARMS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1107640 INSULIN PUMP AUTOMATED INSULIN DOSING DEVICE SYSTEM, SINGLE HORMONAL CONTROL OZP MEDTRONIC MINIMED, INC. 780 G

    Patients

    Seq Age Sex Outcome Treatment
    1 Male APRIDRA VILE.| CENTRUM SILVER MULTI VITAMIN.| DOCUSATE SODIUM 100MG.| DUTASTERIDE 0.5 MG CP.| ELIQUIS (APIXABAN) 5MG.| ESZOPICLONE 1MG.| FESOTERODINE (TOVIAZ) 8MG.| FISH OIL 1200MG.| FLUOXETINE 20 MG| KERENDIA 10NG.| LIVALO 2MG.| MEDTRONIC MINIMED 780G.| METROPROLOL ER SUCCINATE 25MG.| OZEMPIC 1 MG.| PANTOPRAZOLE 40 MG.| PREGABALIN 100MG.| PRESERVISION AREDS 2.| TAMSULOSIN .4 MG TAB.| VITAMIN C 500MG.| VITAMIN D3 5000IU.