# FDA recall Z-1555-2025

> **GE Medical Systems, LLC** · Class II · device recall initiated 2025-03-06.

## Product

Venue Go Models: R2 (Model Number H45181VG), R3 (Model Number H45193VG), R4 (Model Number H45114VG), R5 (Model Numbers H45135VG, H45135VGW), R3 Surgery for China (Model Number H45113VGSU), R3 PeriOP for China (Model Number H45113VGPO), R3 Expert for China (Model Number H45113VGEX ), R3 Pro for China (Model Number H45113VGPR), R3 Performance for China, R3 Intervention for China, R3 Surgery for China (Model Number H45113VGSU) diagnostic ultrasound systems

## Reason for recall

The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-1555-2025
- **Recalling firm:** GE Medical Systems, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-06
- **Report date:** 2025-04-23

- **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-1555-2025

## Citation

> AI Analytics. FDA recall Z-1555-2025. Retrieved 2026-07-28 from https://api.ai-analytics.org/recall/Z-1555-2025. Source: US FDA. Licensed CC0.

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