BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNK PRODUCT

    MDR report key: 2033367 · Received March 22, 2011

    Report

    Report Number
    1831750-2011-02681
    Event Type
    Malfunction
    Date Received
    March 22, 2011
    Date of Event
    February 22, 2011
    Report Date
    February 22, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END WOULD NOT GO UP. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 NA