BEUDAMED
    FDA Adverse Event Death Summary report: N

    SENTRY 1200

    MDR report key: 424272 · Received October 24, 2002

    Report

    Report Number
    1058219-2002-00001
    Event Type
    Death
    Date Received
    October 24, 2002
    Date of Event
    August 31, 2002
    Report Date
    October 24, 2002
    Manufacturer
    SENTECH MEDICAL SYSTEMS, INC.
    Product Code
    FNM
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    PT FOUND WITH THEIR HEAD AND SHOULDERS BETWEEN THE SIDERAILS. PT WAS "UNRESPONSIVE" AND 911 WAS CALLED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SENTRY 1200 PRESSURE RELIEF MATTRESS SYSTEM FNM SENTECH MEDICAL SYSTEMS, INC. SENTRY 1200 LAL *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death