Centricity Universal Viewer recall, credentials at risk
FDA: Device Recalls Class II
Summary
Centricity Universal Viewer recall, credentials at risk
Archived snapshot
Apr 9, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
GE Medical Systems, LLC
Device Recalls (Class II)
← All Device Recalls (Class II) Class II Z-1570-2026 · 20260325 · Ongoing
Product
Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406...
Reason for Recall
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.
Distribution
Worldwide - US Nationwide distribution.
Source: openFDA Enforcement API
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Source
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