---
title: "GE Centricity Universal Viewer Zero Footprint. To view, communicate, process,... — FDA record Z-1333-2022 | Is It on Recall"
description: "Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP)"
url: https://isitonrecall.com/recall/fda-device-z-1333-2022-ge-centricity-universal-viewer-zero-footprint-to-view-communicate-process-and-display-medical-images/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# GE Centricity Universal Viewer Zero Footprint. To view, communicate, process, and display Medical images and data wit... — FDA record Z-1333-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 8, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP)
- **Classification**: Class II
- **Recalling firm**: GE Healthcare, LLC
- **Quantity**: 1,934 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1333-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1333-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI 00840682102988, Versions 6.0 SP6 through SP11.4 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jul 13, 2022
- **Recall initiation date**: Jun 8, 2022
- **Center classification date**: Jul 5, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1333-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [GE Healthcare, LLC records](https://isitonrecall.com/brand/ge-healthcare-llc/)