BEUDAMED
    FDA Adverse Event Other Summary report: N

    FORTE

    MDR report key: 295703 · Received September 8, 2000

    Report

    Report Number
    2916556-2000-00330
    Event Type
    Other
    Date Received
    September 8, 2000
    Date of Event
    August 11, 2000
    Report Date
    August 25, 2000
    Manufacturer
    ADAC LABORATORIES
    Product Code
    KPS
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO ADAC THAT THE CAMERA SENSORS DID NOT STOP THE RADIUS DRIVE MOTOR OF THE ANTERIOR DETECTOR WHEN THE COLLIMATOR CAME IN CONTACT WITH THE PT LOWER ABDOMEN. THERE WAS NO INJURY ASSOCIATED WITH THIS REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FORTE NUCLEAR MEDICINE EQUIPMENT KPS ADAC LABORATORIES 2155-3001B NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *