BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSPORT SERIES OBS

    MDR report key: 2191632 · Received July 1, 2011

    Report

    Report Number
    1831750-2011-06697
    Event Type
    Malfunction
    Date Received
    July 1, 2011
    Date of Event
    June 6, 2011
    Report Date
    June 6, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: BRAKE ADJUSTER.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOTEND BRAKE WOULD NOT LOCK. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSPORT SERIES OBS WHEELED STRETCHER FPO STRYKER MEDICAL 0721 9607030256

    Patients

    Seq Age Sex Outcome Treatment
    1