BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FERNO 35X AMBULANCE STRETCHER

    MDR report key: 2920183 · Received October 26, 2012

    Report

    Report Number
    1523574-2012-00030
    Event Type
    Malfunction
    Date Received
    October 26, 2012
    Date of Event
    August 1, 2012
    Report Date
    October 26, 2012
    Manufacturer
    FERNO-WASHINGTON, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    LOCKING MECHANISMS IS WORN AND UNIT SHOWS NEGLECT AND LACK OF REGULAR MAINTENANCE.

    Description of Event or Problem · 1

    ISSUES WITH STRETCHER LOWERING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FERNO 35X AMBULANCE STRETCHER FERNO 35X AMBULANCE STRETCHER FPO FERNO-WASHINGTON, INC. 35X

    Patients

    Seq Age Sex Outcome Treatment
    1