# FDA recall Z-2317-2026

> **GE Medical Systems, LLC** · Class II · device recall initiated 2026-04-20.

## Product

Allia IGS Pulse angiographic X-ray system

## Reason for recall

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-2317-2026
- **Recalling firm:** GE Medical Systems, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-20
- **Report date:** 2026-06-17

- **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-2317-2026

## Citation

> MORVS. FDA recall Z-2317-2026. Retrieved 2026-10-17 from https://api.morvs.ai/recall/Z-2317-2026. Source: US FDA. Licensed CC0.

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