BEUDAMED
    FDA Adverse Event Death Summary report: N

    CHAMBER, HYPERBARIC

    MDR report key: 21326740 · Received February 6, 2025

    Report

    Report Number
    MW5165704
    Event Type
    Death
    Date Received
    February 6, 2025
    Report Date
    February 1, 2025
    Manufacturer
    SECHRIST INDUSTRIES, INC.
    Product Code
    CBF
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    THE COMPLAINANT ALLEGES THAT A CHILD WAS KILLED AS THE RESULT OF A HYPERBARIC CHAMBER FIRE. I DO NOT KNOW THE SPECIFIC DEVICE INVOLVED IN THE ADVERSE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    622609 CHAMBER, HYPERBARIC CHAMBER, HYPERBARIC CBF SECHRIST INDUSTRIES, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Death