FDAApril 20, 2026device

Allia IGS 3 Pulse angiographic X-ray system

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

ge medical systems

UPCs

00195278719577

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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