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.
FDA Recall Z-0037-2026 · Posted 2025-10-08
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Recalling FirmCanon Medical System, USA, INC.
Recall StatusOpen, Classified
Product CodeOWB
Date Initiated2025-09-02
Product Quantity8
Reason for Recall
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.
Firm Action
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.
Root Cause
Radiation Control for Health and Safety Act
Distribution Pattern
U.S.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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