Lower risk Medical device recall · FDA · Published October 15, 2021

GE Centricity Viewer: Incomplete Patient Imaging Risk

GE Healthcare recalls Centricity Universal Viewer Zero Footprint Client versions with incomplete patient imaging study display. Affected units may need software update to prevent image display issues.

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

🇺🇸 FDA recall #Z-0329-2022Medical device GE Healthcare ›

Lower-risk recall

There is a potential to display incomplete patient imaging study.

Take action

Contact the company

Recalling firmGE Healthcare, LLC3000 N Grandview Blvd · Waukesha, WI 53188-1615

✎ GovInfoNow plain-language explainer

GE Healthcare is recalling certain versions of their Centricity Universal Viewer software. This version may display incomplete patient imaging studies, which could lead to incorrect medical decisions if not addressed. Read more at govinfonow.com/recall/61676-ge-centricity-viewer-incomplete-patient-imaging-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/61676-ge-centricity-viewer-incomplete-patient-imaging-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0329-2022

Cite this page

“GE Centricity Viewer: Incomplete Patient Imaging Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61676-ge-centricity-viewer-incomplete-patient-imaging-risk. Based on FDA recall #Z-0329-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0329-2022%22&limit=1).

GE Healthcare LLC recalled GE Centricity Universal Viewer Zero Footprint Client devices due to a potential to display incomplete patient imaging study, according to the FDA. The agency announced the voluntary Class II recall on Oct. 15, 2021.

How to tell if you have it

GE Healthcare
GE Centricity Universal Viewer Zero Footprint Client
Versions 6.0 SP9, SP9.0.1, SP9.0.1.1, SP9.0.1.2, SP9.0.1.3, SP9.0.1.4, SP9.0.1.5, SP10, SP10.1, SP10.2, SP10.2.1, SP10.2.1.1, SP10.2.2, SP10.2.2.1
GTIN 00840682102988
UDI 00840682102988
UPC 00840682102988

The hazard

The devices have a potential to display incomplete patient imaging study, according to the FDA.

Context

GovInfoNow's records show GE Healthcare LLC has 97 other recalls on record since Oct. 4, 2017. Other recent recalls of similar products include GE Healthcare SIGNA Premier MRI Scanners May Have Steel Fittings Risking Injury (Feb. 27, 2026), GE Centricity Universal Viewer 6.0/7.0/8.0: Inaccurate Distance Measurements (July 15, 2022), and GE Healthcare SIGNA Premier MRI Scanner Recall: Risk of Hearing Loss from Acoustic Noise (June 24, 2022). Other recent recalls of similar products include GE Healthcare Centricity Universal Viewer Zero Footprint Client Recall: Patient Info Mismatch Risk (Jan. 16, 2026), GE Healthcare Centricity PACS Software Recall: Patient Data Mismatch Risk (July 31, 2026), and GE Healthcare Centricity PACS Server V7 Recall: Risk of Wrong Patient Images (July 31, 2026).

How to tell if you have this one

Check if your Centricity Universal Viewer Zero Footprint Client is version 6.0 SP9 through SP10.2.2.1. The product has GTIN 00840682102988 and UDI 00840682102988.

Brand
GE Healthcare
Product
GE Healthcare, LLC recalls GE Centricity Universal Viewer Zero Footprint Client
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Software Version
Identify your software version by checking the Centricity Universal Viewer Zero Footprint Client settings.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 35 states.

FDA distribution: “Worldwide distribution - US Nationwide distribution in the states of AR, AZ, CA, CO, DE, FL, GA, IL, IN, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NJ, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, WA, and WV. The countries of…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Arizona, Arkansas, California, Colorado, Delaware, Florida, Georgia, Illinois, Indiana, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, Nevada, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Washington, West Virginia.

Recall timeline

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

Oct 15, 2021Firm started the recall
Dec 2, 2021FDA classified it Class II
Dec 8, 2021Published in FDA’s Enforcement Report

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

Similar recalls

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Keep exploring

More GE Healthcare recalls

Link to this recall

<a href="https://govinfonow.com/recall/61676-ge-centricity-viewer-incomplete-patient-imaging-risk">GE Centricity Viewer: Incomplete Patient Imaging Risk (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-0329-2022 (October 15, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0329-2022 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.