BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RECOVERY ROOM STRETCH OBS 5/97

    MDR report key: 2043167 · Received March 15, 2011

    Report

    Report Number
    1831750-2011-02490
    Event Type
    Malfunction
    Date Received
    March 15, 2011
    Date of Event
    February 15, 2011
    Report Date
    February 15, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THERE WAS A BROKEN FOOT BRAKE PEDAL. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RECOVERY ROOM STRETCH OBS 5/97 HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1510 NA

    Patients

    Seq Age Sex Outcome Treatment
    1