BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ST104 TRANSPORT

    MDR report key: 1853039 · Received September 21, 2010

    Report

    Report Number
    1831750-2010-02507
    Event Type
    Malfunction
    Date Received
    September 21, 2010
    Date of Event
    July 30, 2010
    Report Date
    August 25, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MX
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: SUPPORT TUBE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT, THE BUNK AND BUNK SUPPORTS HAVE A LOT OF MOVEMENT. THE PISTON HAS A LOT OF MOVEMENT BETWEEN THE PISTON ROD AND THE UPPER NECK. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ST104 TRANSPORT HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MEDICAL DIV. 0737 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA