This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen and lower extremities.
Recall
- Recall Number
- Z-0037-2026
- Event Number
- 97589
- Firm
- Canon Medical System, USA, INC.
- FEI Number
- 2020563
- Product Code
- OWB
- Status
- Open, Classified
- Root Cause
- Radiation Control for Health and Safety Act
- Initiated
- September 2, 2025
- Posted
- October 8, 2025
- Address
- 2441 Michelle Dr, Tustin, CA, 92780-7047
Description
This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen and lower extremities.
It has been found that when SPOT Fluoro is first turned on, the default ROI is selected and the collimator blades move to the boundary of the ROI, and the static image is overlayed around the ROI, covering the collimated area. If the customer changes the ROI, the collimator blades and static images are adjusted accordingly. However, when the acquisition program is changed, the collimator returns to the default ROI position which may be larger than the specified one, leaving the X-ray area partially covered by the static image. This is a software problem with the SPOT Fluoro program and will not occur if the function is not used.
Letters prepared and emailed to notify the customer of the defect. The letter contains a return reply form that is to be completed by the customer and emailed to CMSU for retention.
U.S.
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