BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BATHLIFT BLISS RECLINER US AB

    MDR report key: 3142228 · Received May 23, 2013

    Report

    Report Number
    3005536958-2013-00010
    Event Type
    Malfunction
    Date Received
    May 23, 2013
    Date of Event
    November 1, 2012
    Report Date
    May 21, 2013
    Manufacturer
    HANDICARE
    Product Code
    FNG
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    GA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    THE BATHLIFT WAS USED BY THE CUSTOMER IN THE BATH TUB. THE BATHLIFT OPERATED CORRECTLY LOWERING INTO THE BATH BY DEPRESSING THE DOWN BUTTON ON THE HAND CONTROL. WHEN REQUIRED TO RISE UP OUT OF THE TUB THROUGH OPERATION OF THE UP BUTTON ON THE HAND CONTROL, THE BATHLIFT WOULD NOT OPERATE ON OCCASION. THE CUSTOMER WAS ABLE TO GET OUT OF THE BATH TUB AND NO INJURIES WERE REPORTED AS A RESULT OF THE FAILURE. THE HANDSET HAS CURRENTLY BEEN RECALLED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    229533 BATHLIFT BLISS RECLINER US AB BATHLIFT, 311 FNG HANDICARE 311

    Patients

    Seq Age Sex Outcome Treatment
    1