BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ-PRO R4 AMBUL COT OBS(5/08)

    MDR report key: 1874406 · Received October 12, 2010

    Report

    Report Number
    1831750-2010-02729
    Event Type
    Malfunction
    Date Received
    October 12, 2010
    Date of Event
    September 9, 2010
    Report Date
    September 9, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION ONGOING. LEGS NOT LOCKING.

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT THE COT LEGS WERE UNABLE TO EXTEND AND LOCK INTO POSITION. NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EZ-PRO R4 AMBUL COT OBS(5/08) STRETCHER, WHEELED FPO STRYKER CORP., MEDICAL DIV. 6092 NA

    Patients

    Seq Age Sex Outcome Treatment
    1