BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 3123198 · Received May 21, 2013

    Report

    Report Number
    3004493922-2013-01104
    Event Type
    Malfunction
    Date Received
    May 21, 2013
    Report Date
    April 24, 2013
    Manufacturer
    INVACARE SUZHOU
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MS, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    PROVIDER STATES THE 9099P HYDRAULIC PUMP ON A 9805P HYDRAULIC LIFT IS NOT HOLDING THE LOAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    224267 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9805P

    Patients

    Seq Age Sex Outcome Treatment
    1 Other