BEUDAMED
    FDA Adverse Event Death Summary report: N

    *

    MDR report key: 259315 · Received January 6, 2000

    Report

    Report Number
    2431497-2000-00001
    Event Type
    Death
    Date Received
    January 6, 2000
    Date of Event
    October 3, 1999
    Report Date
    January 5, 2000
    Manufacturer
    SKIL-CARE CORP.
    Product Code
    FMQ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    LA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    RESIDENT DIED IN BED WHILE USING A VEST.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * VEST FMQ SKIL-CARE CORP. UNK *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death