CENTRICITY UNIVERSAL VIEWER ZFP CLIENT 6.0Recalls & reported problems

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

8 FDA recall records name this device's identifier, 6 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

1. Jan 16, 2026Open, Classified

   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,

   Z-1475-2026 · Root cause: Device Design · Recall details · FDA record ↗

2. Oct 3, 2024Open, Classified

   GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) where there is a potential security vulnerability which could allow a malicious actor to access the system and potentially manipulate patient data.

   Z-0318-2025 · Root cause: Software Manufacturing/Software Deployment · Recall details · FDA record ↗

3. Aug 29, 2024Open, Classified

   GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) version v6.0 SP11.x where the latest report is not shown by default to the user. The issue may occur when a study has multiple DICOM structured reports (i.e. preliminary, final, and/or addendum) stored in different series.

   Z-0039-2025 · Root cause: Process control · Recall details · FDA record ↗

4. Jul 23, 2024Open, Classified

   Footprint Client (ZFP) versions v6.0 SP9.x and SP10.x where the latest addended report is not shown by default to the user. The issue occurs when the addendum is created on the same day as the original report but at a different time, and only when launched on the following browsers. " Internet Explorer 10 (IE10) " Internet Explorer 11 (IE11) " Firefox.

   Z-3160-2024 · Root cause: Software Design Change · Recall details · FDA record ↗

5. Jun 8, 2022Open, Classified

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

   Z-1333-2022 · Root cause: Software design · Recall details · FDA record ↗

6. Apr 28, 2022Open, Classified

   Potential for Distance and Area measurements to display inaccurate measurement values when performed on magnified images, and specific to ZFP, Distance and Area measurements can display inaccurate measurement values when performed on lossy images that are scaled down from their original resolution.

   Z-1229-2022 · Root cause: Software design · Recall details · FDA record ↗

7. Oct 15, 2021Terminated

   There is a potential to display incomplete patient imaging study.

   Z-0329-2022 · Root cause: Software design · Recall details · FDA record ↗

8. Nov 9, 2018Terminated

   Issue #1 affects Software Versions 6.0 SP7, SP7.0.1, SP7.0.2, SP7.0.3, SP8, SP8.0.1, SP8.0.a and SP8.0.2. When an image is flipped horizontally and vertically, the orientation markers appear correctly on the image to which they were applied. However, once new image rendering happens on this image or series (with scrolling; playing cin; maximizing or changing viewports/layouts; or synchronizing viewports and resizing the browser), the new image orientation is correctly maintained but the display of orientation markers can become incorrect. Issue #2 affects Software Versions 6.0 SP7, SP7.0.1, SP7.0.2, SP7.0.3, SP8, SP8.0.1, SP8.0.a, SP8.0.2, SP9 and SP9.0.1. When an image in a series is flipped and then rotated in Zero Footprint Viewer (ZFP), the orientation markers appear correctly on the image to which they were applied. However, once you navigate to another image in the series and the image you navigated to has a different orientation than the prior image from which you navigated, the new image orientation is correctly maintained but the display of orientation markers can become incorrect.

   Z-0641-2019 · Root cause: Software design · Recall details · FDA record ↗