# FDA recall Z-1485-2025

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

## Product

GE Healthcare Centricity Radiology RA600 (RA600), Model Numbers:    1) 2022296-001;   2) 2033901-001;   3) 2038437-001;   4) 2038437-011;   5) 2038437-012;   6) 2038437-013;   7) 2038437-014;   8) 2038437-0XX;   9) 2098071-004;   10) 2109571-002;   11) 2109571-006;   12) 2109571-010;   13) 2109594-009;   14) 2109594-011;   15) K2090PS;   16) K2090PTED;   17) MANLEGACY114;   18) MANLEGACY64.

## 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-1485-2025
- **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-1485-2025

## Citation

> AI Analytics. FDA recall Z-1485-2025. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1485-2025. Source: US FDA. Licensed CC0.

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