Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Brilliance iCT Product Usage: Computed Tomography X-ray systems intended to Recalled by Philips Medical Systems (Cleveland) Inc Due to Failure to correctly document the installation of four...
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 Medical Systems (Cleveland) Inc directly.
Affected Products
Brilliance iCT Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories
Quantity: 1
Why Was This Recalled?
Failure to correctly document the installation of four M12 Bolts into the system rotor.
Where Was This Sold?
The one system was distributed in Canada. There were no government or US distribution.
About Philips Medical Systems (Cleveland) Inc
Philips Medical Systems (Cleveland) Inc has 313 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report