# FDA recall Z-0155-2026

> **GE Medical Systems, LLC** · Class II · device recall initiated 2025-09-18.

## Product

LOGIQ P10 series with software version R4.5.7 Model Number   5877534

## Reason for recall

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

## Distribution

US Nationwide. Global Distribution.

## Key facts

- **Recall number:** Z-0155-2026
- **Recalling firm:** GE Medical Systems, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-09-18
- **Report date:** 2025-10-22

- **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-0155-2026

## Citation

> AI Analytics. FDA recall Z-0155-2026. Retrieved 2026-07-25 from https://api.ai-analytics.org/recall/Z-0155-2026. Source: US FDA. Licensed CC0.

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