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.
Enforcement
- Recall Number
- Z-0037-2026
- Event ID
- 97589
- Classification
- Class II
- Status
- Ongoing
- Product Type
- Devices
- Firm
- Canon Medical System, USA, INC.
- Voluntary / Mandated
- FDA Mandated
- Report Date
- October 15, 2025
- Initiation Date
- September 2, 2025
- Classification Date
- October 8, 2025
- Address
- 2441 Michelle Dr, Tustin, CA, 92780-7047, United States
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.
Serial Numbers: SZA2422001, SXA2432001, SUC23Z2014, BBF2392003, SUC2392013, SZA2422002, SXA2432002, SZA2442004.
U.S.
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