BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OMNIPOD 5 PODS

    MDR report key: 23671950 · Received November 28, 2025

    Report

    Report Number
    3004464228-2025-59461
    Event Type
    Malfunction
    Date Received
    November 28, 2025
    Date of Event
    November 4, 2025
    Report Date
    November 28, 2025
    Manufacturer
    INSULET CORPORATION
    Product Code
    QFG
    UDI-DI
    20385083000579
    PMA / PMN Number
    K231826
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    THE DEVICE HAS NOT BEEN RETURNED/RECEIVED TO DATE. IF THE DEVICE IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED WITH THE INVESTIGATION RESULTS. LOT RELEASE RECORDS WERE REVIEWED, AND THE PRODUCT LOT MET ALL ACCEPTANCE CRITERIA. WE ARE UNABLE TO CONFIRM OR DETERMINE THE ROOT CAUSE OF THE REPORTED DISLODGED CANNULA. LOCKED DOWN SMARTPHONE: PHONE CONTROL ANDROID. OMNIPOD SOFTWARE APP VERSION: 3.1.1. OPERATING SYSTEM: TP1A.220624. 014. N981USQSEHYH1. HARDWARE: SM-N981U. CGM SENSOR TYPE: G7. PLEASE NOTE, THE DEVICE IDENTIFIERS ARE CAPTURED AS REPORTED BY THE COMPLAINANT AND MAY NOT ALIGN WITH THE DEVICE CONFIGURATION REPORTED IN THIS SECTION AS THIS DATA IS PULLED FROM OUR CLOUD BASED ON THE REPORTED DATE OF EVENT.

    Description of Event or Problem · 0

    IT WAS REPORTED THE PATIENT'S BLOOD GLUCOSE LEVEL ROSE GREATER THAN 250 MG/DL WHILE WEARING THE POD BETWEEN 1 AND 4 HOURS. THE ADHESIVE COMPLETELY SEPARATED FROM THE (ABDOMEN) AFTER THE PATIENT HAD SHOWERED, CAUSING THE CANNULA TO DISLODGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2266436 OMNIPOD 5 PODS OMNIPOD 5 PODS QFG INSULET CORPORATION PT-001662 PH1U07182541 20385083000579

    Patients

    Seq Age Sex Outcome Treatment
    1 42 YR Female