# FDA recall Z-3038-2026

> **GE Medical Systems Information Technologies Inc** · Class II · device recall initiated 2026-07-20.

## Product

PORTRAIT CORE SERVICES SOFTWARE V1.0.5, Ref# 5697353

## Reason for recall

Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or care area.

## Distribution

US:  MI, NY and Australia, Czech Republic, Finland, Germany, Italy, Netherlands, Qatar, Saudi Arabia, Switzerland, United Arab Emirates, United Kingdom.

## Key facts

- **Recall number:** Z-3038-2026
- **Recalling firm:** GE Medical Systems Information Technologies Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-20
- **Report date:** 2026-09-02

- **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-3038-2026

## Citation

> MORVS. FDA recall Z-3038-2026. Retrieved 2026-10-20 from https://api.morvs.ai/recall/Z-3038-2026. Source: US FDA. Licensed CC0.

---

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