# FDA device recall: GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system

> recall · VERIFIED · 2026-07-10

Firm: GE Medical Systems Information Technologies Inc · Class II · A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed patient alarms, and/or access to Protected Hea

- Company: GE Medical Systems Information Technologies Inc
- Sector: medical devices
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

---
Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.