BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FLUOROSCOPY STRETCHER

    MDR report key: 1830066 · Received September 7, 2010

    Report

    Report Number
    1831750-2010-02114
    Event Type
    Malfunction
    Date Received
    September 7, 2010
    Date of Event
    August 13, 2010
    Report Date
    August 13, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT THERE WAS OIL LEAKING FROM THE BOTTOM OF THE STRETCHER. IT WAS REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT AND THERE WERE NO ADVERSE CONSEQUENCES ASSOCIATED WITH THE REPORTED ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLUOROSCOPY STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIV. 1080 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA