Change Healthcare Radiology Software Version 14.2.2 May Not Display Reports Correctly
Change Healthcare recalls software version 14.2.2 where radiology reports might not show fully. Affected users should check version numbers and contact support for updates.
Lower-risk recall
Due to software issue, radiology reports may not be fully displayed when viewing.
Contact the company
What happened, in plain English
Change Healthcare is recalling a specific software version for radiology systems because reports might not display completely. This could lead to incomplete medical information being used by healthcare providers. Read more at govinfonow.com/recall/51613-change-healthcare-radiology-software-version-14-2-2-may-not.
Source Summary by GovInfoNow · govinfonow.com/recall/51613-change-healthcare-radiology-software-version-14-2-2-may-not · Updated August 17, 2026 · FDA enforcement record: FDA #Z-0030-2026
Cite this page
“Change Healthcare Radiology Software Version 14.2.2 May Not Display Reports Correctly.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51613-change-healthcare-radiology-software-version-14-2-2-may-not. Based on FDA recall #Z-0030-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0030-2026%22&limit=1).
Why it’s dangerous
The software issue causes radiology reports to not display fully when viewed. This means healthcare providers might see incomplete information, potentially affecting patient care decisions.
Who’s affected
Healthcare providers using Change Healthcare Radiology Solutions software version 14.2.2 are most at risk. This affects medical facilities that rely on this software for radiology reports.
How to tell if you have this one
Check if your software version is 14.2.2. The unique identifier (UDI) for this version is (01)17540262030068.
- Brand
Change Healthcare- Product
Change Healthcare Radiology Solutions software version 14.2.2- Category
Medical device
What to do — step by step
Check Software Version
Verify your software version is 14.2.2 by checking the version number in your system settings.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 10 states.
FDA distribution: “Worldwide - US Nationwide distribution in the states of AR, WI, NJ, IN, AL, CA, WA, FL, MA, LA and the country of Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Arkansas, California, Florida, Indiana, Louisiana, Massachusetts, New Jersey, Washington, Wisconsin.
Recall timeline
FDA published this recall 56 days 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-0030-2026 (August 13, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0030-2026 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.