BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 4093704 · Received September 16, 2014

    Report

    Report Number
    3008262382-2014-01086
    Event Type
    Malfunction
    Date Received
    September 16, 2014
    Report Date
    August 21, 2014
    Manufacturer
    INVACARE REHABILITATION EQUIP
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    CUSTOMER ALLEGES THAT THE PUMP HAS NEVER WORKED RIGHT. WHEN PATIENT IS IN THE 9805 HYDRAULIC LIFT IT WILL GRADUALLY LOWER ON ITS OWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    573020 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE REHABILITATION EQUIP 9805

    Patients

    Seq Age Sex Outcome Treatment
    1 Other