BEUDAMED
    FDA Adverse Event Death Summary report: N

    LTV 1200

    MDR report key: 23463732 · Received November 4, 2025

    Report

    Report Number
    23463732
    Event Type
    Death
    Date Received
    November 4, 2025
    Date of Event
    September 17, 2025
    Report Date
    September 26, 2025
    Manufacturer
    VYAIRE MEDICAL, INC.
    Product Code
    CBK
    Adverse Event
    Yes
    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

    TRANSPORT VENTILATOR WHEELS LOCKED UP DURING TRANSPORT AND TUGGED ON ET [ENDOTRACHEAL] TUBE WITH POTENTIAL DISPLACEMENT. PT HAD RESPIRATORY DECOMPENSATION AND ULTIMATELY EXPIRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2546355 LTV 1200 VENTILATOR, CONTINUOUS, FACILITY USE CBK VYAIRE MEDICAL, INC. LTV 1200 15162292

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Female Death