GE Medical Systems recalls Allia IGS 3 Pulse angiographic X-ray systems with potential electrical shock risk during installation or maintenance. Affected units have specific serial numbers and UDI-DI codes.
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 3 Pulse angiographic X-ray systems due to a potential electrical cable issue that could cause shock to service personnel during maintenance. This recall affects specific units with known serial numbers and UDI-DI codes.
An 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 working on these X-ray systems during installation, maintenance, or troubleshooting are most at risk. The recall applies to specific units with known serial numbers and UDI-DI codes.
Check for serial numbers starting with M3-24- or M3-25- or M3-26- in the list provided. The UDI-DI code 00195278719577 also identifies affected units.
Do not perform installation, maintenance, or troubleshooting inside the C-FRT cabinet while the system is powered on.
An electrical cable issue 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.
Units with 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 and UDI-DI 00195278719577.
The recall record does not specify a return or repair process.
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-2314-2026 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-2314-2026 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.
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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.
