BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MICROAIRE®

    MDR report key: 23424549 · Received October 30, 2025

    Report

    Report Number
    23424549
    Event Type
    Malfunction
    Date Received
    October 30, 2025
    Date of Event
    October 16, 2025
    Report Date
    October 16, 2025
    Manufacturer
    MICROAIRE SURGICAL INSTRUMENTS LLC
    Product Code
    QPB
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    WI
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    WHILE OPENING FOR A CASE THE ROOM STAFF NOTED THAT THE STILL SEALED MICROAIRE CANNULA WAS BENT AND UNUSABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1618076 MICROAIRE® SYSTEM, SUCTION, LIPOPLASTY FOR REMOVAL QPB MICROAIRE SURGICAL INSTRUMENTS LLC PAL-308LS 105418052025

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown