Lower risk Medical device recall · FDA · Published January 16, 2026

GE Healthcare Centricity Universal Viewer Zero Footprint Client Recall: Patient Info

GE Healthcare recalls Centricity Universal Viewer Zero Footprint Client models 2110344-039, 2110344-046, 2110344-047 due to potential patient information mismatch in certain workflows with specific software versions.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1475-2026Medical device GE Healthcare ›

Lower-risk recall

Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP) with versions ZFP v6.0: SP11.6, SP11.6.0.1 and SP11.6.1 on systems with Patient Timeline installed,

Take action

Contact the company

Recalling firmGE Healthcare500 W Monroe St · Chicago, IL 60661-3671

✎ GovInfoNow plain-language explainer

GE Healthcare is recalling three specific models of their Centricity Universal Viewer Zero Footprint Client software. The issue may cause patient information shown in the viewer to not match images displayed on the system when using certain software versions with Patient Timeline installed. This could lead to incorrect patient information being displayed during medical imaging workflows. Read more at govinfonow.com/recall/50149-ge-healthcare-centricity-universal-viewer-zero-footprint-client-recall-patient.

Source Summary by GovInfoNow · govinfonow.com/recall/50149-ge-healthcare-centricity-universal-viewer-zero-footprint-client-recall-patient · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1475-2026

Cite this page

“GE Healthcare Centricity Universal Viewer Zero Footprint Client Recall: Patient Info.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/50149-ge-healthcare-centricity-universal-viewer-zero-footprint-client-recall-patient. Based on FDA recall #Z-1475-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1475-2026%22&limit=1).

The FDA announced on Jan. 16, 2026, that GE Healthcare is recalling its Centricity Universal Viewer Zero Footprint Client software due to a hazard where patient information may not match displayed images. The agency issued the Class II recall for systems running specific versions with Patient Timeline installed.

How to tell if you have it

GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 2110344-046, 2110344-047
Versions ZFP v6.0: SP11.6, SP11.6.0.1 and SP11.6.1 on systems with Patient Timeline installed

The hazard

Context

GovInfoNow's records show GE Healthcare has 12 other recalls on record since 2025-02-19. Other recent recalls of similar products include GE Healthcare Centricity PACS Software Recall (2026-07-31), GE Healthcare Centricity Cardiology CA1000: Security Vulnerability Risk (2025-02-19), and GE Healthcare Centricity Universal Viewer Zero Footprint Security Vulnerability Recall (2024-10-03). Other recent recalls of similar products include GE Medical Systems Portrait Compute V1.2 Software Recall (2026-07-20), GE HealthCare ViewPoint 6 Recall (2025-11-03), and GE Medical Systems Portrait Core Services Software V1.1 Recall (2026-07-20).

How to tell if you have this one

Check if your Centricity Universal Viewer Zero Footprint Client has model numbers 2110344-039, 2110344-046, or 2110344-047. The software version must be ZFP v6.0 with specific service packs (SP11.6, SP11.6.0.1, or SP11.6.1) and Patient Timeline installed.

Brand
GE Healthcare
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Software Version
Verify your software version is ZFP v6.0 with service packs SP11.6, SP11.6.0.1, or SP11.6.1 and Patient Timeline installed.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “Worldwide distribution - US Nationwide and the countries of Belarus, Brazil, Canada, China, France, Georgia, Germany, India, Indonesia, Ireland, Israel, Italy, Japan, Korea (Republic Of), Kuwait, Lebanon, Malaysia, Netherlands,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 54 days after the firm started it.

Jan 16, 2026Firm started the recall
Feb 27, 2026FDA classified it Class II
Mar 11, 2026Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Keep exploring

More GE Healthcare recalls

Link to this recall

<a href="https://govinfonow.com/recall/50149-ge-healthcare-centricity-universal-viewer-zero-footprint-client-recall-patient">GE Healthcare Centricity Universal Viewer Zero Footprint Client Recall: Patient Info (GovInfoNow)</a>

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-1475-2026 (January 16, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1475-2026 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.