GE Medical Systems recalls Allia IGS Pulse angiographic X-ray systems with potential electrical shock risk for service personnel 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 Pulse angiographic X-ray systems due to a potential electrical shock hazard for service personnel during installation or maintenance. This risk occurs when technicians work inside the C-FRT cabinet while the system is powered on.
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 hazard occurs during installation, maintenance, or troubleshooting activities.
Service technicians and maintenance personnel who work with the Allia IGS Pulse X-ray systems are most at risk. The recall affects specific units with serial numbers starting with DVMSS2500001HL through DVMSS2600002HL.
Check for serial numbers starting with DVMSS2500001HL through DVMSS2600002HL on the Allia IGS Pulse angiographic X-ray systems. The UDI-DI code 00195278827647 also identifies affected units.
Look for serial numbers starting with DVMSS2500001HL through DVMSS2600002HL on the X-ray system.
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.
Check for serial numbers starting with DVMSS2500001HL through DVMSS2600002HL or the UDI-DI code 00195278827647.
The recall does not specify a remedy, so affected service personnel should follow standard safety protocols and contact GE Medical Systems for further guidance.
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-2317-2026 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-2317-2026 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.
