BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 3143725 · Received June 3, 2013

    Report

    Report Number
    1525712-2013-04301
    Event Type
    Malfunction
    Date Received
    June 3, 2013
    Report Date
    May 6, 2013
    Manufacturer
    UNKNOWN
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    PER FACILITY LIFT KEEPS PUTTING THE PATIENT TO THE FLOOR, CUSTOMER HUNG UP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    243575 NON AC-POWERED PATIENT LIFT 880.5510 FSA UNKNOWN UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Other