Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to GE HealthCare has become aware of the potential...

Date: March 18, 2024
Company: GE Medical Systems, SCS
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact GE Medical Systems, SCS directly.

Affected Products

GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems

Quantity: 1 unit

Why Was This Recalled?

GE HealthCare has become aware of the potential that adhesive material might not have been applied to some bolts of certain Innova IGS, Discovery IGS, Interact IGS, Allia IGS and Allia Pulse IGS products. This could result in a potential fall of the Detector/Elevator or X-ray tube of the frontal Gantry assembly.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About GE Medical Systems, SCS

GE Medical Systems, SCS has 12 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report