BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRIO MOBILE SURGY PLTFRM

    MDR report key: 2221389 · Received August 16, 2011

    Report

    Report Number
    1831750-2011-08747
    Event Type
    Malfunction
    Date Received
    August 16, 2011
    Date of Event
    July 19, 2011
    Report Date
    July 19, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    EVAL RESULT: HEAD PIECE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD ASSEMBLY WAS LOCKING OR PIVOTING INCORRECTLY. THE CUSTOMER COULD NOT DETERMINE IF THERE WAS PT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRIO MOBILE SURGY PLTFRM HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1033 NA

    Patients

    Seq Age Sex Outcome Treatment
    1