BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    30 INCH TRANSPORT

    MDR report key: 1890555 · Received October 29, 2010

    Report

    Report Number
    1831750-2010-03397
    Event Type
    Malfunction
    Date Received
    October 29, 2010
    Date of Event
    October 4, 2010
    Report Date
    October 4, 2010
    Manufacturer
    STRYKER CORP. MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT IS REPORTED BY SERVICE REPORT THAT THE FOOT END JACK IS LEAKING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 30 INCH TRANSPORT HOSPITAL WHEELED STRETCHER FPO STRYKER CORP. MEDICAL DIV. 738 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK