Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0318-2025 — GE Healthcare Centricity Universal Viewer Zero Footprint, Model Numbers: 1) 2089507-083, GDZH-JINWAN-Centricity 2) 2089507-093, 10510-3-Centricity Universal Viewer Zero Footprint / ZFP-02268286, 10510-3-Centricity Universal Viewer Zero Footprint / ZFP-02030900, 1495-1-Centricity Universal Viewer

U.S. FDA — Device Enforcement · United States · 2024-10-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0318-2025
Date of alert
2024-10-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Healthcare
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00840682102988
Reported risk: GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) where there is a potential security vulnerability which could allow a malicious actor to access the system and potentially manipulate patient data.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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