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FDA (Device enforcement)Recalled 2026-04-20class ii

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

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.

Details from the source

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. Quantity: 3 units Lot/code info: UDI-DI: 00198953052488; Serial Numbers: C4-25-001, C4-25-002, C4-26-001, C4-26-002, C4-26-004, C4-26-005

UPC codes

00198953052488

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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