BEUDAMED
    FDA Adverse Event Summary report: N

    MAXILIFT

    MDR report key: 19730 · Received January 3, 1995

    Report

    Report Number
    MW4000639
    Date Received
    January 3, 1995
    Date of Event
    December 26, 1994
    Report Date
    January 3, 1995
    Manufacturer
    ARJO-CENTURY, INC.
    Product Code
    FNG
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    NO INFORMATION

    Narratives

    Description of Event or Problem · 1

    WHILE TRANSFERRING RESIDENT TO WHEELCHAIR ELECTRONIC LIFT MALFUNCTIONED AND WOULD NOT LOWER PROPERLY. PT ASSISTED BACK TO BED WHEN LIFT BAR CAME DOWN TO HER KNEES. HAD PURPLE AREA 1" LONG ON LEFT TOP THIGH. ICE PACK APPLIED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MAXILIFT PT LIFT FNG ARJO-CENTURY, INC. 212000-06

    Patients

    Seq Age Sex Outcome Treatment
    1 *