FDA-Device2026-06-17Class IIPROCESSING DEFECT

GE HealthCare Allia Moveo X-ray system recalled for electrical shock risk to service personnel

ELECTRICAL SHOCKNationwide distribution

GE Allia Moveo X-ray system recalled for electrical shock risk

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.

  • 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
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.

Sold states
Worldwide - US Nationwide distribution.
Affected count
3 units
Manufactured in
3000 N Grandview Blvd, N/A, Waukesha, WI, United States
Products
Allia Moveo angiographic X-ray system

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2318-2026

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