BEUDAMED
    FDA Adverse Event Death Summary report: N

    SECHRIST INDUSTRIES

    MDR report key: 1613745 · Received February 16, 2010

    Report

    Report Number
    1613745
    Event Type
    Death
    Date Received
    February 16, 2010
    Date of Event
    February 21, 2010
    Report Date
    February 12, 2010
    Manufacturer
    SECHRIST INDUSTRIES
    Product Code
    CBF
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    IL, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PATIENT HAVING HBO TREATMENT FOR RIGHT FOOT OSTEOMYELITIS, S/P METATARSAL AMPUTATION. PATIENT DEVELOPED GRAND-MAL SEIZURE AND WAS DECOMPRESSED. HE DEVELOPED AGONAL RESPIRATIONS AND CPR BEGUN IMMEDIATELY AFTER REMOVAL FROM CHAMBER. ACLS ADMINISTERED SUCCESSFULLY, BUT LATER TROPONIN 18.66, EF 16% AND PATIENT DIAGNOSED WITH ACUTE ANOXIC ENCEPHALOPATHY. COMFORT CARE ONLY PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECHRIST INDUSTRIES HBO CHAMBER CBF SECHRIST INDUSTRIES 3200R

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR Death