Reported Jun 17, 2026 · Ongoing
Allia IGS 7 Pulse angiographic X-ray system
GE Medical Systems, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: GE Medical Systems, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615
Is this the product you have?
- Allia IGS 7 Pulse angiographic X-ray system
- Lot codes and dates
- UDI-DI00195278719720
- Serial Numbers
D3-23-024D3-23-029D3-24-001D3-24-002D3-24-005D3-24-006D3-24-008D3-24-009D3-24-010D3-24-013D3-24-014D3-24-016D3-24-019D3-24-020D3-24-021D3-24-023D3-24-025D3-25-001D3-25-002D3-25-003D3-25-005D3-25-006D3-25-007D3-25-008D3-25-009D3-25-010D3-25-013D3-25-016D3-25-017D3-25-018D3-25-026D3-25-027D3-25-029D3-25-030D3-25-034D3-25-036D3-25-037D3-26-001D3-26-002D3-26-007
- Amount recalled
- 35 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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