Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Precision 500D The Precision 500D R&F X-ray System is intended Recalled by GE Healthcare, LLC Due to There has been a reported incident of a...
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 Healthcare, LLC directly.
Affected Products
Precision 500D The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic examinations, including general R&F and pediatric examinations.
Quantity: 825 (38 US and 787 OUS) in total
Why Was This Recalled?
There has been a reported incident of a Distar CRT monitor that has fallen off the monitor wall mount related to product aging.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE Healthcare, LLC
GE Healthcare, LLC has 474 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report