---
title: "The INFX-8000F is designed to take advantage of the latest technological inno... — FDA record Z-1155-2024 | Is It on Recall"
description: "VAREX changed the manufacturing of the internal board, and the detectors displayed abnormal images. Internal board of the X-ray flat panel detector may display"
url: https://isitonrecall.com/recall/fda-device-z-1155-2024-the-infx-8000f-is-designed-to-take-advantage-of-the-latest-technological-innovations-to-reduce-dose/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# The INFX-8000F is designed to take advantage of the latest technological innovations to reduce dose and to save time.... — FDA record Z-1155-2024

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 Nov 15, 2023. 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**: The INFX-8000F is designed to take advantage of the latest technological innovations to reduce dose and to save time. A revolutionary graphic user interface and a multi-tasking computer enable the system to fully meet the requirement for optimum image quality, safety, ease of use, advanced efficiency and improved workflow. The advanced floormounted system INFX-8000F uses a new flat panel detector to present fluoroscopic and fluorographic images of high quality.
- **Reason**: VAREX changed the manufacturing of the internal board, and the detectors displayed abnormal images. Internal board of the X-ray flat panel detector may display abnormal images, such as horizontal stripes, which may lead to the inability to complete an ongoing exam, or the patient may need to be examined with another x-ray system.
- **Classification**: Class II
- **Recalling firm**: Canon Medical System, USA, INC.
- **Quantity**: 2
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1155-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1155-2024%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 | UDI-DI: 04987670100208. Serial Number: BGE2292016, BGE2362017 |

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

## Distribution

US: CA, LA

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Louisiana](https://isitonrecall.com/state/louisiana/)

## Dates in the source

- **Report date**: Feb 28, 2024
- **Recall initiation date**: Nov 15, 2023
- **Center classification date**: Feb 16, 2024

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-1155-2024%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/)