BEUDAMED
    FDA Adverse Event Death Summary report: N

    HOYER LIFT

    MDR report key: 10451386 · Received August 25, 2020

    Report

    Report Number
    3009402404-2020-00030
    Event Type
    Death
    Date Received
    August 25, 2020
    Date of Event
    June 11, 2020
    Report Date
    August 14, 2020
    Manufacturer
    JOERNS HEALTHCARE
    Product Code
    FSA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    501

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO THE MANUFACTURER, BY THE END USER, PER THE END USER, THAT THE PATIENT WAS BEING TRANSFERRED FROM BED TO GERI-CHAIR PER ONE HOSPICE AID VIA FACILITIES HOYER LIFT AND FELL OUT OF SLING. PATIENT WAS TRANSPORTED TO LOCAL HOSPITAL FOR EVALUATION. ADMINISTRATOR STATED THIS INCIDENT WAS DUE TO USER ERROR AND EMPLOYEE DID NOT DOUBLE CHECK TO MAKE SURE THAT THE SLING WAS FULLY CONNECTED. MORE TRAINING HAS BEEN DONE WITH STAFF TO ENSURE THAT THE EXACT PROTOCOL IS BEING USED WITH THE SLINGS AND LIFTS. COMPLAINT #(B)(4) WAS ENTERED INTO OUR SYSTEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    914811 HOYER LIFT HPL700 FSA JOERNS HEALTHCARE HPL700

    Patients

    Seq Age Sex Outcome Treatment
    1 96 YR Death| L