Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Centricity Universal Viewer 7.0 Recalled by GE Healthcare, LLC Due to A software anomaly exists in the Centricity Universal...

Date: August 12, 2021
Company: GE Healthcare, LLC
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact GE Healthcare, LLC directly.

Affected Products

Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system

Quantity: 49

Why Was This Recalled?

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).

Where Was This Sold?

This product was distributed to 8 states: AR, IL, ME, MS, NE, NJ, NY, TN

Affected (8 states)Not affected

About GE Healthcare, LLC

GE Healthcare, LLC has 474 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report