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...
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
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