GE Centricity Universal Viewer Zero Footprint: Inaccurate Medical Image Measurements Risk
GE Healthcare recalls Centric: Universal Viewer Zero Footprint software versions 6.0 SP6 to SP11.4 due to potential inaccurate medical image measurements. Affected users should contact GE for details.
Lower-risk recall
Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP)
Contact the company
What happened, in plain English
GE Healthcare is recalling its Centricity Universal Viewer Zero Footprint software versions 6.0 SP6 through SP11.4 because it may display inaccurate measurements on medical images. This could lead to incorrect medical decisions if the software is used for critical imaging tasks. Read more at govinfonow.com/recall/60530-ge-centricity-universal-viewer-zero-footprint-inaccurate-medical-image-measurements.
Source Summary by GovInfoNow · govinfonow.com/recall/60530-ge-centricity-universal-viewer-zero-footprint-inaccurate-medical-image-measurements · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1333-2022
Cite this page
“GE Centricity Universal Viewer Zero Footprint: Inaccurate Medical Image Measurements Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60530-ge-centricity-universal-viewer-zero-footprint-inaccurate-medical-image-measurements. Based on FDA recall #Z-1333-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1333-2022%22&limit=1).
Why it’s dangerous
The software may display inaccurate measurements on medical images, which could lead to incorrect medical decisions if the software is used for critical imaging tasks. This is a software issue that affects the accuracy of measurements in medical imaging systems.
Who’s affected
Healthcare professionals using GE Centricity Universal Viewer Zero Footprint software versions 6.0 SP6 through SP11.4 for medical imaging. Those handling critical medical images are most at risk.
How to tell if you have this one
Check if you have GE Centricity Universal Viewer Zero Footprint software versions 6.0 SP6 through SP11.4. The software is used for viewing, communicating, processing, and displaying medical images within a computer network or workstation.
- Brand
GE Healthcare- Category
Medical device
What to do — step by step
Contact GE Healthcare
Reach out to GE Healthcare for specific instructions on how to address the issue with your software version.
How this recall unfolded
Recall timeline
FDA published this recall 35 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-1333-2022 (June 8, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1333-2022 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.