# FDA recall Z-1483-2025

> **GE Healthcare** · Class II · device recall initiated 2025-02-19.

## Product

GE Healthcare Centricity Universal Viewer (UV), Model Numbers: 1) 2066908-077;   2) 2066908-136;   3) 2066908-150;   4) 2088026-003;   5) 2088026-026;   6) 2088026-032;   7) 2088026-043;   8) 2088026-110;   9) 2088026-115;   10) 2088026-132;   11) 2088026-306;   12) 2088026-308;   13) 2088026-406;   14) 2088026-506;   15) 2088026-614;   16) 2088026-713;   17) 2088026-714;   18) 2088026-715;   19) 2088026-723;   20) 2088026-806;   21) 2088026-906;   22) 2088026-936;   23) 2088026-940;   24) 2088026-943;   25) 2088026-946;   26) 2088026-948;   27) 2088026-957;   28) 2088026-959;   29) 2088026-960;   30) 2088026-961;   31) 2088026-962;   32) 2088026-967;   33) 2088026-969;   34) 2088026-970;   35) 2088026-971;   36) 2088026-973;   37) 2088026-985;   38) 2088026-989;   39) 2088026-990;   40) 2088026-993;   41) 2088026-994;   42) 2089629-003;   43) 2100169-001;   44) 2100491-006;   45) 2100491-012;   46) 2102675-010;   47) 2102675-101;   48) 2102676-001;   49) 2104867-001;   50) 2104867-044

## 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.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1483-2025
- **Recalling firm:** GE Healthcare
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-19
- **Report date:** 2025-04-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chicago, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1483-2025

## Citation

> AI Analytics. FDA recall Z-1483-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1483-2025. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*