# FDA recall Z-1333-2022

> **GE Healthcare, LLC** · Class II · device recall initiated 2022-06-08.

## Product

GE Centricity Universal Viewer Zero Footprint.   To view, communicate, process, and display Medical images and data within a computer network or on a workstation.

## Reason for recall

Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP)

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1333-2022
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-06-08
- **Report date:** 2022-07-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1333-2022

## Citation

> AI Analytics. FDA recall Z-1333-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1333-2022. Source: US FDA. Licensed CC0.

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