Recall
FDAHealthApril 20, 2026

GE Medical Systems, LLC — Allia Moveo angiographic X-ray system

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
April 20, 2026

Worldwide - US Nationwide distribution.

What's affected?

Product
Allia Moveo angiographic X-ray system
Lot code
UDI-DI: 00198953052488; Serial Numbers: C4-25-001, C4-25-002, C4-26-001, C4-26-002, C4-26-004, C4-26-005

Additional details

UDI-DI: 00198953052488; Serial Numbers: C4-25-001, C4-25-002, C4-26-001, C4-26-002, C4-26-004, C4-26-005

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 3 units.

View original FDA notice →

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