Allia IGS Pulse angiographic X-ray system
FDA Recall Z-2317-2026 · Posted 2026-06-05
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Recalling FirmGE Medical Systems, LLC
Recall StatusOpen, Classified
Product CodeOWB
Date Initiated2026-04-20
Product Quantity5 units
Reason for Recall
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.
Firm Action
An URGENT MEDICAL DEVICE CORRECTION dated 4/20/26 was sent to customers.
Actions to be taken by Customer/User
You can continue to use your system.
As a reminder, qualified service personnel must follow the Service Manual applicable to your system and use the appropriate personal protective equipment (PPE) for electrical hazards when performing any activity inside the cabinet while power is ON.
If any abnormal condition is observed on the Iris Power Cable during servicing, such as loose or visibly exposed wires, qualified service personnel must follow the Electrical Lockout/Tagout Procedure as described in Service Manual.
Please ensure that all potential users and service personnel in your facility are made aware of this safety notification and the recommended actions and post this letter in a visible location near the C-FRT cabinet.
Please retain this document for your records.
Please complete and return the attached acknowledgement form electronically via FMI 18014 Digital Response Form or print, fill out manually, scan, and email to
[email protected].
Root Cause
Device Design
Distribution Pattern
Worldwide - US Nationwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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