Class II

Medical Device Recall: Allia IGS 3 Pulse angiographic X-ray system

GE Medical Systems, LLC · April 20, 2026

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.

States Affected

NATIONWIDE

Quantity Affected

9 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2314-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

GE Medical Systems, LLC Medical Device Recall: Allia IGS 3 Pulse angiographic X-ray system | SafeCheck