GE Healthcare Centricity PACS Software Version 7.0 SP0.14 Recall: Study Modification
GE Healthcare recalls Centricity PACS software version 7.0 SP0.0.4.7 due to failure to process study modification notifications on post-verified exams. Affected units include model 5831882-012 with GTIN 00840682145572.
Lower-risk recall
The Event Notification Manager (ENM) functionality for certain products does not process notifications for study modifications performed on post verified exams.
Contact the company
What happened, in plain English
GE Healthcare is recalling Centricity PACS software version 7.0 SP0.0.4.7 because it fails to process notifications for study modifications on post-verified exams. This could lead to missing critical updates in medical imaging systems, potentially affecting patient care. Read more at govinfonow.com/recall/60507-ge-healthcare-centricity-pacs-software-version-7-0-sp0-14.
Source Summary by GovInfoNow · govinfonow.com/recall/60507-ge-healthcare-centricity-pacs-software-version-7-0-sp0-14 · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1466-2022
Cite this page
“GE Healthcare Centricity PACS Software Version 7.0 SP0.14 Recall: Study Modification.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60507-ge-healthcare-centricity-pacs-software-version-7-0-sp0-14. Based on FDA recall #Z-1466-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1466-2022%22&limit=1).
Why it’s dangerous
The software fails to process notifications when study modifications are made after exams have been verified. This means critical updates to imaging studies might not be reflected in the system, potentially causing errors in patient records or treatment plans.
Who’s affected
Healthcare facilities using the recalled software version are affected. Medical staff handling imaging studies may be at risk if notifications for study modifications are not processed correctly.
How to tell if you have this one
Check if your Centricity PACS software is version 7.0 SP0.0.4.7 with model number 5831882-012 or GTIN 00840682145572. The software was sold with these specific identifiers.
- Brand
GE Healthcare- Product
GE Healthcare, LLC recalls Centricity PACS Software Version 7.0 SP0.0.4.7- Category
Medical device
What to do — step by step
Check Software Version
Verify your Centricity PACS software version by checking the model number or GTIN on the device.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 5 states.
FDA distribution: “Worldwide distribution - US Nationwide distribution in the states of CO, NV, OH, PA, WA and the countries of Brazil, Canada, China, France, Germany, Israel, Italy, Japan, Oman, Spain, Switzerland, and United Kingdom.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Colorado, Nevada, Ohio, Pennsylvania, Washington.
Recall timeline
FDA terminated this recall 19 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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-1466-2022 (June 14, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1466-2022 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.