BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ST104 TRANSPORT

    MDR report key: 1853055 · Received September 21, 2010

    Report

    Report Number
    1831750-2010-02489
    Event Type
    Malfunction
    Date Received
    September 21, 2010
    Date of Event
    August 24, 2010
    Report Date
    August 24, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE STRETCHER IS LEAKING HYDRAULIC FLUID. IT WAS REPORTED THAT THERE WAS A PT INVOLVED, HOWEVER THERE WERE NO ADVERSE CONSEQUENCES REPORTED AS A RESULT OF THIS ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ST104 TRANSPORT HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MEDICAL DIV. 0735 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK