BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 2981841 · Received February 27, 2013

    Report

    Report Number
    1525712-2013-01490
    Event Type
    Malfunction
    Date Received
    February 27, 2013
    Report Date
    January 28, 2013
    Manufacturer
    UNKNOWN
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND

    Narratives

    Description of Event or Problem · 1

    DEALER STATED THAT THE UNKNOWN HYDRAULIC PATIENT LIFT IS GETTING STUCK IN THE RAISED POSITION, WILL NOT LOWER. THIS LIFT IS NOT EQUIPPED WITH AN EMERGENCY RELEASE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    83566 NON AC-POWERED PATIENT LIFT 880.5510 FSA UNKNOWN UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Other