BEUDAMED
    FDA Adverse Event Death Summary report: N

    BEKA

    MDR report key: 20694755 · Received November 15, 2024

    Report

    Report Number
    3007802293-2024-00009
    Event Type
    Death
    Date Received
    November 15, 2024
    Date of Event
    October 21, 2024
    Report Date
    November 14, 2024
    Manufacturer
    BEKA HOSPITEC GMBH
    Product Code
    FSA
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 0

    EMPLOYEE # (B)(6) AND EMPLOYEE #(B)(6) WERE TRANSFERRING RESIDENT FROM BED TO WHEELCHAIR USING THE BEKA LIFT. THE BEKA CARLO LIFTS IS 11 YEARS OLD AND PAST IT RECOMMENDED USABLE LIFE. THE RESIDENT WAS BEING TRANSFERRED IN A LARGE COMFORT CARE SLING. ONE EMPLOYEE WAS USING THE CONTROLS WHILE THE OTHER WAS SUPPORTING THE CLIENT. THE PATIENT WAS BEING TRANSFERRED WHEN THE BOLT CONNECTING THE CARRY BAR TO THE BOOM SHEARED OFF. THE CLIENT FELL FROM THE LIFT WHEN THE CARRY BAR DISENGAGED FROM THE BOOM. THE RESIDENT FELL AND HIT HER HEAD ON THE OPEN LEGS OF THE FLOOR LIFT AND PASSED AWAY FROM THEIR INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1324160 BEKA CARLO FSA BEKA HOSPITEC GMBH 925001008

    Patients

    Seq Age Sex Outcome Treatment
    1 96 YR Female Death