BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SURGISTOOL

    MDR report key: 1811496 · Received August 17, 2010

    Report

    Report Number
    1831750-2010-01841
    Event Type
    Malfunction
    Date Received
    August 17, 2010
    Date of Event
    June 21, 2010
    Report Date
    June 21, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FZM
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT THE JACK IS DRIFTING. NO ADVERSE CONSEQUENCES WERE ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SURGISTOOL STOOL, OPERATING-ROOM FZM STRYKER CORP., MEDICAL DIVISION 0830 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA