BEUDAMED
    FDA Adverse Event Other Summary report: N

    SM204 M-SERIES W/BIG WHEEL

    MDR report key: 1001455 · Received February 19, 2008

    Report

    Report Number
    1831750-2008-00015
    Event Type
    Other
    Date Received
    February 19, 2008
    Date of Event
    September 27, 2007
    Report Date
    January 17, 2008
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ME, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED THAT THE STRETCHERS BRAKES WORK INTERMITTENTLY.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Required Intervention