BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 4243646 · Received November 11, 2014

    Report

    Report Number
    3008262382-2014-01952
    Event Type
    Malfunction
    Date Received
    November 11, 2014
    Report Date
    October 23, 2014
    Manufacturer
    INVACARE REHABILITATION EQUIP
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    CAREGIVER STATES THAT END USER'S LIFT JUST HAD A PUMP REPLACED 2-3 DAYS AGO AND SINCE THEN, THE HANGER IS REAL HARD TO PUSH DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    727021 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE REHABILITATION EQUIP 9805

    Patients

    Seq Age Sex Outcome Treatment
    1 Other