Allia Moveo angiographic X-ray system
Pending LLM rewrite. Source: FDA_DEVICE Z-2318-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
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.
The recalled product
- Product
- Allia Moveo angiographic X-ray system
- Manufacturer
- GE Medical Systems, LLC
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (7)
- UDI-DI: 00198953052488
- Serial Numbers: C4-25-001
- C4-25-002
- C4-26-001
- C4-26-002
- C4-26-004
- C4-26-005
Distribution
Distributed nationwide across the United States.
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