BEUDAMED
    FDA Adverse Event Other Summary report: N

    HOYER LIFT

    MDR report key: 1883400 · Received September 16, 2010

    Report

    Report Number
    2182305-2010-00038
    Event Type
    Other
    Date Received
    September 16, 2010
    Date of Event
    August 17, 2010
    Report Date
    September 16, 2010
    Manufacturer
    APEX HEALTHCARE MFG INC
    Product Code
    FNG
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO MFR BY FACILITY; (B)(4), PER FACILITY, THEY WERE POSITIONING THE LIFT ABOVE THE RESIDENT IN PREPARATION FOR A TRANSFER WHEN THE LIFT ARM ALLEGEDLY GAVE WAY AND LANDED ON THE RESIDENT'S STOMACH. NO FURTHER INFO HAS BEEN GIVEN BY THE FACILITY AT THIS TIME REGARDING THE CURRENT STATE OF THE RESIDENT. THEY ARE REQUESTING THE JOERNS SEND A NEW LIFTER TO THEM AND COME OUT TO INSPECT THE LIFT IN QUESTION AS SOON AS POSSIBLE. (B)(4). AFTER CUSTOMER / FACILITY REC'D THE NEW LIFT THAT THE MFR SENT, THEY ARE ALL SET AND DO NOT NEED JOERNS TO EVALUATE THE LIFT ALLEGEDLY INVOLVED IN THE REPORTED INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HOYER LIFT PATIENT LIFTER FNG APEX HEALTHCARE MFG INC PRESENCEWSC

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other