Use caution Medical device recall · FDA · Published April 27, 2023

NRT X-RAY Intelli-C Left Tabletop Recall: Drive Shaft Break Risk

NRT X-RAY recalls Intelli-C Left side suspended Tabletop models with serial numbers 647009, 651002, 651006, 666009, 682003 due to potential drive shaft breakage causing detector movement.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1669-2023Medical device NRT X-RAY ›

Use caution until it’s fixed

There is a potential that the drive shaft in the detector up/down (IDE) movement of the X-Ray machine may break which causes the detector to move until it is stopped by the movement end-stop.

Take action

Contact the company

Recalling firmNRT X-RAY A/SBirkegardsvej 16 · Hasselager, Denmark

✎ GovInfoNow plain-language explainer

NRT X-RAY is recalling specific Intelli-C Left side suspended Tabletop X-ray machines that may have a drive shaft that breaks, causing the detector to move until stopped. This could lead to improper X-ray imaging or safety risks if the machine malfunctions during use. Read more at govinfonow.com/recall/58492-nrt-x-ray-intelli-c-left-tabletop-recall-drive-shaft.

Source Summary by GovInfoNow · govinfonow.com/recall/58492-nrt-x-ray-intelli-c-left-tabletop-recall-drive-shaft · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1669-2023

Cite this page

“NRT X-RAY Intelli-C Left Tabletop Recall: Drive Shaft Break Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/58492-nrt-x-ray-intelli-c-left-tabletop-recall-drive-shaft. Based on FDA recall #Z-1669-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1669-2023%22&limit=1).

The FDA announced on April 27, 2023, that NRT X-RAY A/S is recalling its Intelli-C Left side suspended Tabletop (REF: 03400010) due to a potential drive shaft breakage hazard. The agency classified the recall as Class II.

How to tell if you have it

Brand: NRT X-RAY
Product: Intelli-C, Left side suspended Tabletop
REF: 03400010
UDI-DI: 05713464000121
Serial Numbers: 647009, 651002, 651006, 666009, 682003

The hazard

According to the FDA, the drive shaft in the detector up/down (IDE) movement of the X-Ray machine may break. This failure causes the detector to move until it is stopped by the movement end-stop.

Context

GovInfoNow's records show NRT X-RAY A/S has issued two other recalls since January 21, 2022, including an April 17, 2024 recall for uncontrolled C-arm motion risk and a January 21, 2022 recall regarding missing friction blocks in footrests. Other recent recalls of similar products include the Shimadzu Ceiling X-Ray Tube Support Models CH-200/CH-200M Recall dated October 16, 2025, the Canon Alphenix X-ray Systems Recall dated August 4, 2026, and the GE Optima XR220amx Mobile X-Ray System Recall dated June 5, 2026.

How to tell if you have this one

Check for serial numbers 647009, 651002, 651006, 666009, or 682003 on the Intelli-C Left side suspended Tabletop X-ray machines. The recall applies to specific models sold by NRT X-RAY.

Brand
NRT X-RAY
Category
Medical device

FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
US Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, LA, NV, NY.

Recall number	Product, codes & lots	Quantity
Z-1668-2023	Intelli-C, Right side suspended Tabletop, REF: 03400000; UDI-DI: 05713464000527/Serial Numbers: 627004, 627007, 639001, 639002,639003, 639004, 639007, 639010, 647001, 647004, 647005, 648001, 651007, 658002, 658003, 658006, 658010, 666008, 675001, 675004, 682006, 682010	32 units
Z-1669-2023	Intelli-C, Left side suspended Tabletop, REF: 03400010; UDI-DI:05713464000121/Serial Numbers: 647009, 651002, 651006, 666009, 682003	13 units

Based on the official FDA remedy

What to do — step by step

Check Serial Numbers
Verify if your X-ray machine has serial numbers 647009, 651002, 651006, 666009, or 682003.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 10 states.

FDA distribution: “US Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, LA, NV, NY.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Iowa, Kentucky, Louisiana, Massachusetts, Nevada, New York, North Carolina, Ohio, South Carolina, Washington.

Recall timeline

FDA published this recall 41 days after the firm started it.

Apr 27, 2023Firm started the recall
May 31, 2023FDA classified it Class II
Jun 7, 2023Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/58492-nrt-x-ray-intelli-c-left-tabletop-recall-drive-shaft">NRT X-RAY Intelli-C Left Tabletop Recall: Drive Shaft Break Risk (GovInfoNow)</a>

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-1669-2023 (April 27, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1669-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.