BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWER PRO AMBULANCE COT

    MDR report key: 1872539 · Received October 8, 2010

    Report

    Report Number
    1831750-2010-02717
    Event Type
    Malfunction
    Date Received
    October 8, 2010
    Date of Event
    September 20, 2010
    Report Date
    September 20, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    OTHER: LEAK.

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED IN A SERVICE REPORT THAT THE COT WAS LEAKING FLUID FROM THE HYDRAULIC FILL PLUG. THERE HAVE BEEN NO ADVERSE CONSEQUENCES REPORTED.

    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