BEUDAMED
    FDA Adverse Event Other Summary report: N

    READY LIFT

    MDR report key: 2667050 · Received March 21, 2007

    Report

    Report Number
    1318912-2007-00001
    Event Type
    Other
    Date Received
    March 21, 2007
    Date of Event
    February 5, 2007
    Report Date
    March 16, 2007
    Manufacturer
    NOR-AM PATIENT CARE PRODUCTS, INC.
    Product Code
    FNG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION REVEALED THE TOP AND BOTTOM CLEVIS WERE ROUNDED AND ELONGATED AFTER YEARS OF USE. FACILITY TO DO MONTHLY MAINTENANCE INSPECTION AND REPLACE ACTUATORS WHEN WEAR IS SHOWN. THE PT WAS BEING TRANSFERRED WITH THE ACTUATOR FULLY EXTENDED. WE BELIEVE THE LIFT WAS BEING TURNED WITH THE PT RAISED IN THE HIGHEST POSITION AND ACTUATOR BEING USED FOR LEVERAGE.

    Description of Event or Problem · 1

    PT WAS BEING TRANSFERRED WITH READY LIFT WITH THE MOTOR PISTON FULLY EXTENDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 READY LIFT FNG NOR-AM PATIENT CARE PRODUCTS, INC. RL-100E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 75 YR