BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SM204 M-SERIES W/BIG WHEEL

    MDR report key: 1958435 · Received December 15, 2010

    Report

    Report Number
    1831750-2010-04881
    Event Type
    Malfunction
    Date Received
    December 15, 2010
    Date of Event
    November 18, 2010
    Report Date
    November 18, 2010
    Manufacturer
    STRYKER CORP, MED DIV
    Product Code
    FPO
    Removal / Correction Number
    Z-228-08
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BRAKE AND STEER FUNCTION WOULD NOT STAY ENGAGED. IT IS UNK IF THERE WAS PT INVOLVEMENT, HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SM204 M-SERIES W/BIG WHEEL HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MED DIV 1015 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK