# FDA recall Z-0918-2025

> **GE Medical Systems, LLC** · Class II · device recall initiated 2024-12-06.

## Product

Portrait Core Services, a set of software services that enable the communication and interaction of the Portrait Mobile Monitoring Solution components and will integrate into existing healthcare facility infrastructure and clinical information systems, Model CSSXB

## Reason for recall

There is a software issue that can result in the loss of patient monitoring on the Portrait Central Viewer Application after 425 days of continuous run-time.

## Distribution

Worldwide - US Nationwide distribution in the states of OH, TX and the countries of Australia, China, Czech Republic, France, Italy, Netherlands, Qatar, Singapore, UAE, UK.

## Key facts

- **Recall number:** Z-0918-2025
- **Recalling firm:** GE Medical Systems, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-12-06
- **Report date:** 2025-01-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0918-2025

## Citation

> AI Analytics. FDA recall Z-0918-2025. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-0918-2025. Source: US FDA. Licensed CC0.

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