BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POSEY SITTER SELECT

    MDR report key: 3140846 · Received May 24, 2013

    Report

    Report Number
    MW5030337
    Event Type
    Malfunction
    Date Received
    May 24, 2013
    Date of Event
    May 22, 2013
    Report Date
    May 24, 2013
    Manufacturer
    POSEY COMPANY
    Product Code
    KMI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PT WAS FOUND OUT OF BED AND THE FALL ALARM WAS NOT ALARMING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    232824 POSEY SITTER SELECT SITTER SELECT FALL ALARM KMI POSEY COMPANY

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR