GE Medical Systems, LLC recalls Allia IGS 3 Pulse angiographic X-ray system
- Recalling company
- GE Medical Systems, LLC
- Product
- Allia IGS 3 Pulse angiographic X-ray system
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 20, 2026
- Reported
- Jun 17, 2026
- Distribution
- Worldwide - US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 9 units
- Lot / codes
- UDI-DI: 00195278719577; Serial Numbers: M3-24-053, M3-24-124, M3-25-029, M3-25-051, M3-25-053, M3-25-091, M3-25-098, M3-25-124, M3-26-010, M3-26-030
- Company location
- Waukesha, WI
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2314-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2314-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.