BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HOYER LIFT INVOLIFT 625

    MDR report key: 17634853 · Received August 25, 2023

    Report

    Report Number
    MW5144998
    Event Type
    Malfunction
    Date Received
    August 25, 2023
    Date of Event
    August 21, 2023
    Report Date
    August 23, 2023
    Manufacturer
    INOVI HEALTHCARE, LLC.
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    003
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    RESIDENT WAS BEING TRANSFERRED WITH HOYER-LIFT FROM BED TO CHAIR, WHEN HOYER-LIFT BROKE (ARM/BRACKET BROKE FREE FROM MACHINE ARM) AND RESIDENT FELL FROM THE HOYER-LIFT TO THE FLOOR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1000116 HOYER LIFT INVOLIFT 625 LIFT, PATIENT, NON-AC-POWERED FSA INOVI HEALTHCARE, LLC.

    Patients

    Seq Age Sex Outcome Treatment
    1 88 YR Unknown