BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ WAY CEILING LIFT

    MDR report key: 8666472 · Received June 4, 2019

    Report

    Report Number
    8666472
    Event Type
    Malfunction
    Date Received
    June 4, 2019
    Date of Event
    April 13, 2019
    Report Date
    April 23, 2019
    Manufacturer
    EZ WAY, INC.
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NY
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    PATIENT WAS BEING TRANSFERRED FROM BED TO WHEELCHAIR USING THE CEILING LIFT USING THE CEILING MOUNTED HOYER SYSTEM. PATIENT WAS LOWERED TO THE CHAIR AND UNHOOKED FROM HOYER. THE STAFF MEMBER ASSISTING WAS MOVING THE HOYER LIFT ASIDE AND THE LIFTING MECHANISM FELL OFF THE RAILS. NO INJURY TO THE PATIENT. WHEN THE LIFT WAS INSPECTED AGAINST ANOTHER LIFT, THE 2 NEW LIFTS WERE MISSING THE GUARDRAIL WHICH PREVENTS THE LIFT FROM COMING OFF THE TRACK. MANUFACTURER WAS NOTIFIED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    461858 EZ WAY CEILING LIFT LIFT, PATIENT, NON-AC-POWERED FSA EZ WAY, INC. CL650MT

    Patients

    Seq Age Sex Outcome Treatment
    1