BEUDAMED
    FDA Adverse Event Death Summary report: N

    MATTRESS LOW AIRLOSS SENTECH P

    MDR report key: 352789 · Received September 20, 2001

    Report

    Report Number
    MW4003090
    Event Type
    Death
    Date Received
    September 20, 2001
    Date of Event
    August 18, 2001
    Report Date
    September 20, 2001
    Manufacturer
    SENTECH MEDICAL SYSTEMS, INC.
    Product Code
    FNM
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT FOUND ON STOMACH, HEAD BETWEEN MATTRESS AND SIDERAIL. MATTRESS WAS DEPRESSED UNDER WEIGHT OF PT. CAUSE OF DEATH DETERMINED BY CORONER TO BE POSITIONAL ASPHYXIA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    42821 MATTRESS LOW AIRLOSS SENTECH P PRIMARY CARE MATTRESS REPLACEMENT SYSTEM FNM SENTECH MEDICAL SYSTEMS, INC. MDTMSENPCLA *

    Patients

    Seq Age Sex Outcome Treatment
    1 85 YR Death VERTICAL SIDING THREE QUARTER BEDSIDE RAIL #2510.