GE Healthcare Centricity Universal Viewer Zero Footprint Client v6.0 SP11.x Report Issue
GE Healthcare recalls Centricity Universal Viewer Zero Footprint Client v6.0 SP11.x where reports aren't shown by default when multiple DICOM structured reports exist in different series.
Lower-risk recall
GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) version v6.0 SP11.x where the latest report is not shown by default to the user. The issue may occur when a study has multiple DICOM structured reports (i.e. preliminary, final, and/or addendum) stored in different series.
Contact the company
What happened, in plain English
GE Healthcare is recalling certain versions of their Centricity Universal Viewer Zero Footprint Client software (v6.0 SP11.x) because it doesn't display all reports by default when multiple DICOM structured reports are stored in different series. This could lead to missing reports in medical imaging systems. Read more at govinfonow.com/recall/54147-ge-healthcare-centricity-universal-viewer-zero-footprint-client-v6-0.
Source Summary by GovInfoNow · govinfonow.com/recall/54147-ge-healthcare-centricity-universal-viewer-zero-footprint-client-v6-0 · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0039-2025
Cite this page
“GE Healthcare Centricity Universal Viewer Zero Footprint Client v6.0 SP11.x Report Issue.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54147-ge-healthcare-centricity-universal-viewer-zero-footprint-client-v6-0. Based on FDA recall #Z-0039-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0039-2025%22&limit=1).
Why it’s dangerous
The software fails to show all reports by default when multiple DICOM structured reports (like preliminary, final, and addendum reports) are stored in different series within a single study. This could cause healthcare providers to miss important reports during patient imaging reviews.
Who’s affected
Healthcare facilities using GE Healthcare Centricity Universal Viewer Zero Footprint Client software version v6.0 SP11.x with the listed model numbers are affected. Medical staff using this software for imaging reports are most at risk.
How to tell if you have this one
Check if your software version is v6.0 SP11.x with any of the listed model numbers (2089507-120 through 2089507-154) or the specific product IDs provided in the recall notice.
- Brand
GE Healthcare- Category
Medical device
What to do — step by step
Check Software Version
Verify your software version is v6.0 SP11.x with any of the listed model numbers (2089507-120 through 2089507-154) or the specific product IDs provided in the recall notice.
How this recall unfolded
Recall timeline
FDA published this recall 48 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-0039-2025 (August 29, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0039-2025 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.