Official recall record
GE Healthcare Centricity Centricity PACS-IW with Universal Viewer, Model Numbers: 1) 2049587-015; 2) 2066908-086; 3) 2066908-136; 4
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2025-02-19
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Brand on record
- GE Healthcare
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2026-07-31 · US FDA — Medical Devices
Centricity PACS V2, V3, V4, V6, V7, software product is intended for the storage, reading, diagnostic review, - 2026-07-31 · US FDA — Medical Devices
Centricity PACS Server V7, intended for managing digital medical images and associated data, All versions - 2026-07-31 · US FDA — Medical Devices
Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electroni
All 13 official recall notices naming GE Healthcare on this site →
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.