Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GE Inspection Technologies Recalled by GE Inspection Technologies, LP Due to GE Inspection Technologies, LP ("GE") has discovered that...
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 Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
Quantity: 55 US Distribution
Why Was This Recalled?
GE Inspection Technologies, LP ("GE") has discovered that certain of its cabinet x-ray systems may not fully comply with the Food and Drug Administration's (FDA) Cabinet X¿ ray System performance standards, 21 C.F.R. ¿ 1020.40(c)(1)(i)
Where Was This Sold?
This product was distributed to 24 states: AL, AZ, CA, CO, FL, GA, ID, IN, MD, MA, MI, MN, NH, NJ, NY, NC, OH, PA, SC, TN, TX, VA, WI, DC
About GE Inspection Technologies, LP
GE Inspection Technologies, LP has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report