Official recall record
Allia IGS 5 Pulse angiographic X-ray system
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-04-20
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00195278719263
- Brand on record
- GE Medical Systems, LLC
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-09-16.
Same barcode in other registries
The same EAN appears in 1 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2024-03-18 · US FDA — Medical Devices
GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems
Other recalls from this brand
- 2026-06-05 · US FDA — Medical Devices
Optima XR200amx, Mobile Digital-Ready Radiographic System - 2026-06-05 · US FDA — Medical Devices
Optima XR240amx, Mobile Digital Radiographic System - 2026-06-05 · US FDA — Medical Devices
Optima XR220amx, Mobile Digital-Ready Radiographic System
All 62 official recall notices naming GE Medical Systems, LLC on this site →