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...
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
About GE Healthcare, LLC
GE Healthcare, LLC has 474 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report