BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EYE SURGERY STRETCHER OBS

    MDR report key: 2010120 · Received March 1, 2011

    Report

    Report Number
    1831750-2011-02063
    Event Type
    Malfunction
    Date Received
    March 1, 2011
    Date of Event
    February 16, 2011
    Report Date
    February 16, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    CRANK FOWLER DURAL ARTICULATING ARM.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER WAS NOT HOLDING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EYE SURGERY STRETCHER OBS HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1069 NA

    Patients

    Seq Age Sex Outcome Treatment
    1