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Medical Device

Allia IGS Pulse angiographic X-ray system

Recall date: 2026-06-17 · Source: FDA_DEVICE
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.
Units affected
5 units
Description
Allia IGS Pulse angiographic X-ray system
View official recall notice →