Recall Z-1487-2025— GE Healthcare
Class II · Ongoing
Class II FDA medical device recall by GE Healthcare, initiated 2025-02-19. FDA's recall record names no specific 510(k) clearance for this event. Product: GE Healthcare Centricity Centricity PACS-IW with Universal Viewer, Model Numbers: 1) 2049587-015; 2) 2066908-086; 3) 2066908-136; 4) 2104867-045.. Reason: There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data..
- Recalling firm
- GE Healthcare
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-02-19
- Firm location
- Chicago, IL, United States
Product description
GE Healthcare Centricity Centricity PACS-IW with Universal Viewer, Model Numbers: 1) 2049587-015; 2) 2066908-086; 3) 2066908-136; 4) 2104867-045.
Reason for recall
There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.
Data sourced from openFDA. This site is unofficial and independent of the FDA.