BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NEPTUNE

    MDR report key: 24303529 · Received February 10, 2026

    Report

    Report Number
    24303529
    Event Type
    Malfunction
    Date Received
    February 10, 2026
    Date of Event
    January 30, 2026
    Report Date
    February 2, 2026
    Manufacturer
    STRYKER CORPORATION
    Product Code
    FYD
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    AZ
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    [REDACTED] 11:14 AM BY RISK,RDE: NEPTUNE (SUCTION MACHINE) STOPPED WORKING IN THE MIDDLE OF THE CASE THEREFORE LEAVING THE SURGICAL FIELD WITHOUT SUCTION. REGISTERED NURSE RAN TO GRAB A REPLACEMENT UNIT. SECOND NEPTUNE MACHINE JUST CLEANED AND REMOVED FROM THE FIELD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    362370 NEPTUNE APPARATUS, EXHAUST, SURGICAL FYD STRYKER CORPORATION 0703001000

    Patients

    Seq Age Sex Outcome Treatment
    1 77 YR Unknown