GE HealthCare Allia Moveo X-ray system recalled for electrical shock risk to service personnel
GE HealthCare identified a potential electrical cable issue on certain Allia Moveo angiographic X-ray systems equipped with Gaia generators. Service personnel who work inside the equipment cabinet while power is on could be exposed to electrical shock during installation, maintenance, or troubleshooting.
From the FDA notice · Read the official notice ↗ · All GE recalls
What to do
- If you operate or service this equipment, contact GE HealthCare immediately for instructions
- Do not perform work inside the C-FRT cabinet while power is on until you receive guidance from the manufacturer
Is yours affected?
Compare your label or packaging with the recalled product.
- Product
- Allia Moveo angiographic X-ray system
- Sold in
- Nationwide
- Made for
- All ages (0 months and older)
This recall covers 5 products — see all of them.
Details
- Units affected
- 3 units
- Illnesses reported
- None reported
- Manufactured in
- 3000 N Grandview Blvd, N/A, Waukesha, WI, United States
- Classification
- Class II
- Recall number
- Z-2318-2026
In the FDA's words
- Description
- 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. UDI-DI: 00198953052488; Serial Numbers: C4-25-001, C4-25-002, C4-26-001, C4-26-002, C4-26-004, C4-26-005 Distribution: Worldwide - US Nationwide distribution. Affected quantity: 3 units
- 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.
5 products in this recall
GE Allia IGS X-ray systems recalled for electrical shock risk
GE HealthCare found a possible problem with an electrical cable in certain Allia IGS X-ray systems that use Gaia generators. The issue could expose service personnel to electrical shock while working inside the C-FRT cabinet with power on. This recall includes 5 product lines, with 173 affected units in total.
The agency lists each product separately. Check every one you might have.
- Allia IGS 3 Pulse angiographic X-ray systemZ-2314-2026 · 9 units
- Allia IGS 5 Pulse angiographic X-ray systemZ-2315-2026 · 121 units
- Allia IGS 7 Pulse angiographic X-ray systemZ-2316-2026 · 35 units
- Allia IGS Pulse angiographic X-ray systemZ-2317-2026 · 5 units
- Allia Moveo angiographic X-ray system (this page)Z-2318-2026 · 3 units
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ModerateFDANov 4, 2026