GE Healthcare: Device Recall

Recall #Z-1487-2025 · 02/19/2025

Class II: Risk

Recall Details

Recall Number
Z-1487-2025
Classification
Class II
Product Type
Device
Recalling Firm
GE Healthcare
Status
Ongoing
Date Initiated
02/19/2025
Location
Chicago, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
4 units

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.

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.

Distribution Pattern

Worldwide distribution.

Other Recalls by GE Healthcare

View all recalls by GE Healthcare →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.