Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CombiDiagnost R90 Image-Intensified fluoroscopic x-ray system CombiDiagnost R90 is a Recalled by Philips Electronics North America Corporation Due to The tube adapter-plate green/yellow protective earthing (PE) wire...
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 Philips Electronics North America Corporation directly.
Affected Products
CombiDiagnost R90 Image-Intensified fluoroscopic x-ray system CombiDiagnost R90 is a multi-functional general R/F system. It is suitable for all routine radiography and fluoroscopy exams, including specialist areas like angiography or pediatric work, excluding mammography
Quantity: 10
Why Was This Recalled?
The tube adapter-plate green/yellow protective earthing (PE) wire was removed. and spacers with different thickness were used to position pre-loc ring in respect to focal spot in specified distance.
Where Was This Sold?
Worldwide Distribution - US Distribution and to the countries of : France, Germany, Luxembourg and New Zealand.
About Philips Electronics North America Corporation
Philips Electronics North America Corporation has 160 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report