BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRETCHER

    MDR report key: 2191843 · Received July 29, 2011

    Report

    Report Number
    1831750-2011-07873
    Event Type
    Malfunction
    Date Received
    July 29, 2011
    Date of Event
    July 1, 2011
    Report Date
    July 1, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE WHEEL IS BROKEN AND WILL NOT ROLL. THE CUSTOMER COULD NOT DETERMINE WHETHER THERE WAS PT INVOLVEMENT OR ADVERSE CONSEQUENCES OCCURRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1010 NA

    Patients

    Seq Age Sex Outcome Treatment
    1