BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 3143754 · Received June 3, 2013

    Report

    Report Number
    9616091-2013-00937
    Event Type
    Malfunction
    Date Received
    June 3, 2013
    Report Date
    May 6, 2013
    Manufacturer
    INVAMEX
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    THE FACILITY IS STATING THAT THE LIFT LOWERS DOWN ON ITS OWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    245015 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVAMEX RPL450-1

    Patients

    Seq Age Sex Outcome Treatment
    1 Other