Use cautionMedical device recall · FDA · Published November 26, 2019
Deerfield Imaging iMRX MRI System Recall: X-ray Failure Risk
Deerfield Imaging recalls iMRX MRI and Angiography Systems with specific part numbers due to potential X-ray tube failure from generator A100 power supply issues. Affected units may not produce X-rays during procedures.
There is a potential hardware error for the iMRX System with a generator A100. A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible
Take action
Contact the company
📍Recalling firmDeerfield Imaging, Inc.5101 Shady Oak Rd S · Minnetonka, MN 55343-4100
“Deerfield Imaging iMRX MRI System Recall: X-ray Failure Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/66428-deerfield-imaging-imrx-mri-system-recall-x-ray-failure-risk. Based on FDA recall #Z-0762-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0762-2020%22&limit=1).
Deerfield Imaging, Inc. recalled the iMRX MRI and Angiography System on Nov. 26, 2019, due to a potential hardware error that may cause generator failure, according to the FDA. The Food and Drug Administration announced the Class II recall of six units distributed in Connecticut, Massachusetts, Virginia, Australia, Canada, and Qatar.
How to tell if you have it
Brand: Deerfield Imaging
Product: iMRX MRI and Angiography System
Part numbers: 10094137 and 10094141
Serial numbers: 146792, 153374, 153642, 153793, 153896, 154588
The hazard
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible.
Context
GovInfoNow's records show Deerfield Imaging, Inc. has had 8 other recalls since Feb. 20, 2018. Other recent recalls of similar products include Philips Allura Cardio Vascular-Allura Centron X-Ray System Recall (June 17, 2026), Philips Azurion 5 M12 X-ray System May Not Start Properly - Recall (March 3, 2026), and Micro-X Rover Mobile X-ray System Recall (March 27, 2026).
How to tell if you have this one
Check for part numbers 10094137 or 10094141 on the iMRX MRI and Angiography System. Affected units have serial numbers including 146792, 153374, 153642, 153793, 153896, or 154588.
Brand
Deerfield Imaging
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check System Part Numbers
Identify if your iMRX system has part numbers 10094137 or 10094141.
Contact Manufacturer
Reach out to Deerfield Imaging for guidance on next steps if your system is affected.
Where it went and when
Where it was distributed
Distributed in 3 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “CT, MA, VA. International distribution: Australia, Canada, and Qatar.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Connecticut, Massachusetts, Virginia.
Recall timeline
FDA terminated this recall 8 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0762-2020 (November 26, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0762-2020 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.