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 Optional Laser Centering Device X-ray generator. Recalled by GE Inspection Technologies, LP Due to GE has identified a potential failure to comply...

Date: November 10, 2014
Company: GE Inspection Technologies, LP
Status: Terminated
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 Inspection Technologies, LP directly.

Affected Products

GE Optional Laser Centering Device X-ray generator.

Quantity: 25

Why Was This Recalled?

GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and 21 C.F.R. ¿ 1010.2 for the alignment laser centering device.

Where Was This Sold?

This product was distributed to 8 states: AL, CA, FL, LA, MD, NY, PA, WA

Affected (8 states)Not affected

About GE Inspection Technologies, LP

GE Inspection Technologies, LP has 7 total recalls tracked by RecallDetector.

Related Recalls

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