The device is an X-ray system that is capable of radiographic and fluoroscopic studies and is used in an interventional setting. The system consists of a C-arm which is equipped with an X-ray tube, beam limiter and X-ray receptor, X-ray controller, computers with system and processing software, and a patient radiographic table.
FDA Recall Z-1154-2024 · Posted 2024-02-16
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Recalling FirmCanon Medical System, USA, INC.
Recall StatusOpen, Classified
Product CodeOWB
Date Initiated2023-11-15
Product Quantity1
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.
Firm Action
On 11/15/23 correction notices were distributed to customers who were asked to do the following:
1) Should this issue occur please attempt to restart the system and contact your service
representative.
2) A recalling firm representative will contact you to schedule a time to replace the flat panel detector on the console. The parts required to address the defect are expected
to be available no earlier that December 2023.
3) Complete and return the customer reply form via email to [email protected]
For questions, please contact our InTouch team at [email protected] or 800-421-1968, or 800.521.1968.
Root Cause
Component change control
Distribution Pattern
US: CA, LA
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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