Ge Medical Systems, Llc: System, Image Processing, Radiological

Recall Summary GE Medical Systems is recalling Centricity Universal Viewer Software (versions 6.0 through 6.0 Sp10.4.1), which is used to display medical images including mammograms and related data. A cybersecurity vulnerability in certain versions may expose user login credentials on workstations, potentially allowing unauthorized access that could affect system availability or alter data. The recall affects medical facilities nationwide that use affected software versions and model numbers.

Recalling firm
GE Medical Systems, LLC
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, 2100169-001, 2088026-985, 2088026-971, 2088026-614, 2088026-713, 2088026-994, 2100491-006, 2088026-723, 2088026-308, 2104867-044, 2100491-012, 2088026-962, 2088026-969, 2102676-001, 2088026-936, 2088026-960, K1220JWED, 2088026-806, 2088026-506, 2088026-026, 2088026-970, 2088026-943, 2088026-990, 2088026-940, 2088026-959, 2088026-967, 2088026-989, 2104867-045, 2088026-993, 2088026-306,...
Reason
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.
Classification
Class II
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-01-30
Status
Open, Classified
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
Worldwide - US Nationwide distribution.

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d74736a9-cf2a-45a1-b793-d2d01b36b261