BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWER PRO AMBULANCE COT

    MDR report key: 1853080 · Received September 21, 2010

    Report

    Report Number
    1831750-2010-02495
    Event Type
    Malfunction
    Date Received
    September 21, 2010
    Date of Event
    August 25, 2010
    Report Date
    August 25, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: LEAK.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT HYDRAULIC FLUID WAS LEAKING AT THE VELOCITY PLUG. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED. INVESTIGATION INTO THIS COMPLAINT IDENTIFIED THAT THE LEAK WAS NOT FROM THE VELOCITY PLUG. THE LEAK ORIGINATED FROM THE HYDRAULIC FILL PLUG WHICH IS LOCATED ON THE SAME END OF THE RAM CYLINDER AS THE VELOCITY FILL PLUG.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POWER PRO AMBULANCE COT STRETCHER WHEELED FPO STRYKER CORP., MEDICAL DIV. 6500 NA

    Patients

    Seq Age Sex Outcome Treatment
    1