BEUDAMED
    FDA Adverse Event Injury Summary report: N

    59T EZ GLIDE STAIR CHAIR

    MDR report key: 4102648 · Received September 10, 2014

    Report

    Report Number
    1523574-2014-00019
    Event Type
    Injury
    Date Received
    September 10, 2014
    Date of Event
    August 15, 2014
    Report Date
    September 10, 2014
    Manufacturer
    FERNO-WASHINGTON, INC.
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE UNIT WAS EVALUATED BY (B)(4), ON BEHALF OF MANUFACTURER, AND NO DEFECTS OR MALFUNCTIONS WERE FOUND. THE UNIT PASSED ALL QUALITY TESTS. THE CUSTOMER CONFIRMED THAT THEY WERE UNABLE TO IDENTIFY ANY ISSUES WITH THE UNIT.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT DURING A TRANSPORT, WHILE DESCENDING THE STAIRS THAT THE UNIT SLID DOWN THE STAIRS AND FELL BACKWARDS TO THE GROUND. THE REPORTED INJURIES WERE EVALUATED AND ALL PARTIES WERE DISCHARGED WITHOUT COMPLAINT FROM THE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    559491 59T EZ GLIDE STAIR CHAIR 59T EX GLIDE STAIR CHAIR FPO FERNO-WASHINGTON, INC. 0731328

    Patients

    Seq Age Sex Outcome Treatment
    1 Other