BEUDAMED
    FDA Adverse Event Death Summary report: N

    POSEY

    MDR report key: 14992 · Received May 14, 1994

    Report

    Report Number
    14992
    Event Type
    Death
    Date Received
    May 14, 1994
    Date of Event
    April 27, 1994
    Report Date
    May 3, 1994
    Manufacturer
    ZIMMER CO.
    Product Code
    FMQ
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    MS, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    RESIDENT WAS FOUND ON FLOOR BESIDE HIS BED WITH RESTRAINT ON AND TIGHT AROUND CHEST AND NECK. CORONER'S REPORT WAS NOT AVAILABLE TO FACILITY UNTIL 5/3/94. THE CAUSE OF DEATH WAS STRANGULATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POSEY VEST RESTRAINT FMQ ZIMMER CO. 3353L

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Death