BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    THE GUARDIAN SYSTEM

    MDR report key: 21834867 · Received April 14, 2025

    Report

    Report Number
    3017374019-2025-00023
    Event Type
    Malfunction
    Date Received
    April 14, 2025
    Date of Event
    November 19, 2024
    Report Date
    April 14, 2025
    Manufacturer
    AVERTIX MEDICAL INC
    Product Code
    QBI
    PMA / PMN Number
    P150009
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    BIOMEDICAL ENGINEER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PREMATURE BATTERY ERI/EOS. THIS IS ONE OF 25 DEVICES THAT HAD THIS ISSUE. THIS MRD IS BEING FILED RETROACTIVELY AT THE REQUEST OF CDRH AND OII AFTER AN INSPECTION OF FEB. 2025. AVERTIX HAD PERFORMED A VOLUNTRAY RECALL/CORRECTION IN 2023 FOR THIS ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1022823 THE GUARDIAN SYSTEM GUARDIAN QBI AVERTIX MEDICAL INC AMSG3-E 121720V0209530000037

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Female Required Intervention