Recall
FDAHealthApril 20, 2026

GE Medical Systems, LLC — Allia IGS Pulse angiographic X-ray system

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
April 20, 2026

Worldwide - US Nationwide distribution.

What's affected?

Product
Allia IGS Pulse angiographic X-ray system
Lot code
UDI-DI: 00195278827647; Serial Numbers: DVMSS2500001HL, DVMSS2500002HL, DVMSS2500003HL, DVMSS2500004HL, DVMSS2500005HL, DVMSS2500006HL, DVMSS2600001HL, DVMSS2600002HL

Additional details

UDI-DI: 00195278827647; Serial Numbers: DVMSS2500001HL, DVMSS2500002HL, DVMSS2500003HL, DVMSS2500004HL, DVMSS2500005HL, DVMSS2500006HL, DVMSS2600001HL, DVMSS2600002HL

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 5 units.

View original FDA notice →

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