Z-1155-2024 Class II Ongoing

Recalled by Canon Medical System, USA, INC. — Tustin, CA

Recall Details

Product Type
Devices
Report Date
February 28, 2024
Initiation Date
November 15, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2

Product Description

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 for Recall

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.

Distribution Pattern

US: CA, LA

Code Information

UDI-DI: 04987670100208. Serial Number: BGE2292016, BGE2362017