CENTRICITY UNIVERSAL VIEWER 7.0Recalls & reported problems

Summary

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

6 FDA recall records name this device's identifier, 4 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

1. Jan 30, 2026Open, Classified

   There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.

   Z-1569-2026 · Root cause: Software design · FDA record ↗

2. Feb 19, 2025Open, Classified

   There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

   Z-1483-2025 · Root cause: Software design · FDA record ↗

3. Sep 8, 2023Open, Classified

   When using Universal Viewer or Centricity Universal Viewer with Workflow Manager (WFM), if a third-party reporting application is used to launch exams, it could display information on a different patient than WFM and the Viewer.

   Z-0142-2024 · Root cause: Software design · FDA record ↗

4. Jul 15, 2022Open, Classified

   Inaccurate Distance and Area measurements with use of Global Stack viewport.

   Z-1566-2022 · Root cause: Process design · FDA record ↗

5. Aug 12, 2021Terminated

   A software anomaly exists in the Centricity Universal Viewer study management feature in which study changes are not propagated to either the Centricity Enterprise Archive (EA) or another Vendor Neutral Archive (VNA).

   Z-0012-2022 · Root cause: Other · FDA record ↗

6. Mar 19, 2021Terminated

   When the Cross Enterprise Display option is enabled on the Centricity Universal Viewer and Workflow Manager option is used as the PACS worklist launching the viewer, the patient jacket may potentially include a different patient s comparison exam(s).

   Z-1533-2021 · Root cause: Under Investigation by firm · FDA record ↗