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