BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    30 INCH TRANSPORT

    MDR report key: 2050880 · Received April 4, 2011

    Report

    Report Number
    1831750-2011-03236
    Event Type
    Malfunction
    Date Received
    April 4, 2011
    Date of Event
    March 7, 2011
    Report Date
    March 7, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE LEFT AND RIGHT UPRIGHT LOCKING SPINDLES ARE BROKEN AND THE SIDERAIL CANNOT BE LATCHED UP. NO PATIENT 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 MEDICAL 0738 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA