Trophy SAS CS9600 X-ray System Recall: Device May Not Function Properly
Trophy SAS recalls CS9600 extraoral X-ray systems that may fail to function as intended, affecting dental and medical imaging for pediatric and adult patients.
Lower-risk recall
Device failed to function as intended and/or failed to conform to their design specifications.
Contact the company
What happened, in plain English
Trophy SAS is recalling its CS9600 extraoral X-ray system because it may not work correctly. This could lead to improper imaging for dental, ENT, cervical spine, and wrist scans in children and adults. Read more at govinfonow.com/recall/62176-trophy-sas-cs9600-x-ray-system-recall-device-may-not.
Source Summary by GovInfoNow · govinfonow.com/recall/62176-trophy-sas-cs9600-x-ray-system-recall-device-may-not · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1627-2023
Cite this page
“Trophy SAS CS9600 X-ray System Recall: Device May Not Function Properly.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62176-trophy-sas-cs9600-x-ray-system-recall-device-may-not. Based on FDA recall #Z-1627-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1627-2023%22&limit=1).
Why it’s dangerous
The device may not function as intended or meet design specifications, which could result in inaccurate imaging. This might affect diagnostic support for patients needing X-ray scans.
Who’s affected
Healthcare professionals who use the CS9600 system for dental, ENT, cervical spine, and wrist imaging in pediatric and adult patients are most at risk.
How to tell if you have this one
The CS9600 extraoral X-ray system is used by healthcare professionals for dental, ENT, cervical spine, and wrist imaging. It was sold for pediatric and adult patients.
- Brand
Trophy SAS- Category
Medical device
What to do — step by step
Check Device Functionality
Verify if the CS9600 system works correctly for producing X-ray images as intended.
How this recall unfolded
Recall timeline
FDA published this recall 23 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1627-2023 (July 21, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1627-2023 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.