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 Radiation emissions which exceeded the limit in the...
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 - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus CT system used primarily for 3D metrology and analysis.
Quantity: 4
Why Was This Recalled?
Radiation emissions which exceeded the limit in the performance standard were detected during maintenance of one system. The identified cause was insufficient attachment of shielding in the door. Jostling during delivery was identified as the probable cause of this failure to comply with the performance standard.
Where Was This Sold?
This product was distributed to 3 states: FL, TN, TX
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