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GE Medical Systems, LLC recalls Allia IGS Pulse angiographic X-ray system
Recalled June 17, 2026 · FDA recall Z-2317-2026 · GE Medical Systems
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. · FDA Class II
Units
5 units
Sold at
Worldwide - US Nationwide distribution.
Description
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.
Product
Allia IGS Pulse angiographic X-ray system
Manufacturer(s)
GE Medical Systems, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →