BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HOYER 600

    MDR report key: 2148843 · Received May 13, 2011

    Report

    Report Number
    9681684-2011-00027
    Event Type
    Malfunction
    Date Received
    May 13, 2011
    Date of Event
    January 7, 2011
    Report Date
    March 15, 2011
    Manufacturer
    BHM MEDICAL, INC.
    Product Code
    FNG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    JOERNS HEALTH CARE MEDWATCH# 2182305-2011-0002. FURTHER INFO WILL BE PROVIDED UPON CONCLUSION OF THE MFR'S INVESTIGATION.

    Description of Event or Problem · 1

    IT WAS REPORTED BY (B)(6), THAT ONE OF THEIR CUSTOMER'S FACILITIES WAS USING THE FLOOR LIFT TO TRANSFER A RESIDENT WHEN THE SCALE AND CRADLE SEPARATED AND THE RESIDENT FELL BACK ONTO THE BED. NO INJURIES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HOYER 600 MANUFACTURED FLOOR PASSIVE LIFT FNG BHM MEDICAL, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Other