GE Medical Systems recalls Allia IGS 7 Pulse angiographic X-ray systems with specific serial numbers due to potential electrical shock risk during installation or maintenance when power is on. Affected units require immediate attention from service personnel.
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.
GE Medical Systems is recalling certain Allia IGS 7 Pulse angiographic X-ray systems because an electrical cable issue could cause electrical shock to service personnel working inside the machine's cabinet while it's powered on. This recall affects specific serial numbers and requires immediate action from service technicians.
The electrical cable on certain IGS systems with Gaia generators could cause electrical shock if service personnel work inside the C-FRT cabinet while the system is powered on. This risk occurs during installation, maintenance, or troubleshooting activities.
Service personnel who install, maintain, or troubleshoot these X-ray systems are most at risk. The recall applies to specific serial numbers of the Allia IGS 7 Pulse angiographic X-ray systems.
Check for the specific serial numbers listed in the recall: D3-23-024 through D3-26-007. The product is an Allia IGS 7 Pulse angiographic X-ray system manufactured by GE Medical Systems.
Service personnel should stop working on the affected system while it's powered on to avoid electrical shock.
The electrical cable on certain IGS systems with Gaia generators could cause electrical shock to service personnel working inside the C-FRT cabinet while the system is powered on.
The affected serial numbers are D3-23-024, D3-23-029, D3-24-001 through D3-26-007 as listed in the recall.
No action is required for end users; this recall is specifically for service personnel working on the system.
We’ve drafted a message you can send GE Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2316-2026 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-2316-2026 from GE Medical Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
