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Recall Observatory FDA recall evidence

Device product

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.

Z-0037-2026

September 02, 2025

Class II

Product summary

Firm
Canon Medical System, USA, INC.
Event
Event 97589
Status
Ongoing
Classification
Class II
Quantity
8
Official record key
device-enforcement:Z-0037-2026

Official wording

Reason: 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.

Code information: Serial Numbers: SZA2422001, SXA2432001, SUC23Z2014, BBF2392003, SUC2392013, SZA2422002, SXA2432002, SZA2442004.

Distribution pattern: U.S.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software problem