ClearanceBrief
Recall Z-0037-2026 ยท OWB Interventional Fluoroscopic X-Ray System

Canon Medical System, USA, INC.

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.

DateOct 8, 2025 (initiated Sep 2, 2025)
StatusOpen, Classified
ReasonIt 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 no
Root causeRadiation Control for Health and Safety Act
ActionLetters 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.
Quantity8
DistributionU.S.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K210900Alphenix, INFX-8000C/B, INFX-8000C/S, V9.2
Canon Medical Systems Corporation, Apr 12, 2021
K233107Alphenix, INFX-8000V/B, INFX-8000V/S, V9.5
Canon Medical Systems Corporation, Aug 30, 2024