# FDA recall Z-1475-2026

> **GE Healthcare** · Class II · device recall initiated 2026-01-16.

## Product

GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers:  2110344-039, 2110344-046, 2110344-047; System, Image Processing, Radiological

## Reason for 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,

## 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, Philippines, Poland, Russia, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkiye, United Arab Emirates, United Kingdom, Vietnam.

## Key facts

- **Recall number:** Z-1475-2026
- **Recalling firm:** GE Healthcare
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-16
- **Report date:** 2026-03-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chicago, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1475-2026

## Citation

> AI Analytics. FDA recall Z-1475-2026. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1475-2026. Source: US FDA. Licensed CC0.

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