BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANTAGE SERIES 26

    MDR report key: 1933129 · Received December 13, 2010

    Report

    Report Number
    1831750-2010-04762
    Event Type
    Malfunction
    Date Received
    December 13, 2010
    Report Date
    November 16, 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 BY SVC REPORT THAT THERE IS NO AIR CIRCULATION ON THE BLADDER AND A SMALL AMOUNT OF OIL FOUND ON THE FLOOR. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADVANTAGE SERIES 26 HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIV. 1001 NA

    Patients

    Seq Age Sex Outcome Treatment
    1