---
title: "This device is a digital radiography/fluoroscopy system used in a diagnostic ... — FDA record Z-0037-2026 | Is It on Recall"
description: "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 stati"
url: https://isitonrecall.com/recall/fda-device-z-0037-2026-this-device-is-a-digital-radiography-fluoroscopy-system-used-in-a-diagnostic-and-interventional-angi/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configura... — FDA record Z-0037-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 2, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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.
- **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.
- **Classification**: Class II
- **Recalling firm**: Canon Medical System, USA, INC.
- **Quantity**: 8
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0037-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0037-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Serial Numbers: SZA2422001, SXA2432001, SUC23Z2014, BBF2392003, SUC2392013, SZA2422002, SXA2432002, SZA2442004. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

U.S.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Oct 15, 2025
- **Recall initiation date**: Sep 2, 2025
- **Center classification date**: Oct 8, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0037-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Canon Medical System, USA, INC. records](https://isitonrecall.com/brand/canon-medical-system-usa-inc/)