BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PATIENT LIFT

    MDR report key: 297388 · Received September 10, 2000

    Report

    Report Number
    1525712-2000-00069
    Event Type
    Malfunction
    Date Received
    September 10, 2000
    Date of Event
    August 1, 2000
    Report Date
    August 30, 2000
    Manufacturer
    INVACARE CORPORATION
    Product Code
    FNG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    DE, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    MFR RECEIVED A REPORT FROM A FACILITY ALLEGING THAT THE SCREWS WHICH HOLDS THE CRADLE TO THE LIFT BACKED OUT WHILE TWO AIDES WERE TRANSFERRING AN ENDUSER, CAUSING THE PT TO FALL. X-RAYS WERE TAKEN BUT NO INJURY OCCURRED, ONLY DISCOMFORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PATIENT LIFT AC-POWERED PATIENT LIFT FNG INVACARE CORPORATION PATIENT LIFT, ELEC NA

    Patients

    Seq Age Sex Outcome Treatment
    1 89 YR