BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ATLAS

    MDR report key: 2091190 · Received April 20, 2011

    Report

    Report Number
    1831750-2011-03801
    Event Type
    Malfunction
    Date Received
    April 20, 2011
    Date of Event
    March 23, 2011
    Report Date
    March 23, 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 SVC REPORT THAT THE FOOT END DRIFTS DOWN AND THE FOOT END SIDERAIL HORN DAMAGED AND MISSING PRESENTING SHARP EDGES. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ATLAS HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 0660 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA