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Medium risk Drugs & MedicationsClass II

GE Medical Systems, LLC Recall

Allia IGS 3 Pulse angiographic X-ray system

Updated April 20, 2026

GE Medical Systems, LLC is recalling Allia IGS 3 Pulse angiographic X-ray system. 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.

Is the GE Medical Systems, LLC recalled? Yes. This product was recalled by FDA on April 20, 2026. Details below.

What is recalled

Allia IGS 3 Pulse angiographic X-ray system

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The 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.

Brands affected

GE Medical Systems, LLC
Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-2314-2026
Classification
Class II
Recalled
April 20, 2026
Read the official notice

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