BEUDAMED
    FDA Adverse Event Summary report: N

    HOYER LIFT

    MDR report key: 727246 · Received June 15, 2006

    Report

    Report Number
    2182305-2006-00018
    Date Received
    June 15, 2006
    Date of Event
    May 16, 2006
    Report Date
    June 5, 2006
    Manufacturer
    APEX HEALTHCARE MFG INC
    Product Code
    FNG
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CLIENT ADVISED THAT THE REPLACEMENT PART ON THE LIFT HAD BROKE CAUSING THE DAUGHTER TO ALL AND FRACTURE HER LEG. MANUFACTURER HAVE BEEN TRYING TO COMMUNICATE WITH THE FAMILY'S ATTORNEY TO ALLOW US TO INSPECT THE LIFT AND THIS ACTUATOR. HOWEVER, THE ATTORNEY HAS NOT CONTACTED THE DEALER OR THEIR ADJUSTER. WE DID REQUEST THAT THE LIFT BE TAKEN OUT OF SERVICE AND REMAIN UN-REPAIRED UNTIL WE ARE ALLOWED TO DO AN INSPECTION OF THIS PRODUCT. THIS IS THE SECOND INCIDENT INVOLVING THE SAME LIFT AND END USER AS ONE MONTH AGO. REFERENCE MDR REPORT# 2182305-2006-0014 DATED 05/05/2006.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other