Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips CT systems labeled as the following: 1. Brilliance iCT SP Recalled by Philips North America Llc Due to The patient support table (couch) may descend unexpectedly...
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 North America Llc directly.
Affected Products
Philips CT systems labeled as the following: 1. Brilliance iCT SP, Model Number: 728311.
Quantity: 14 units
Why Was This Recalled?
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America Llc
Philips North America Llc has 301 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report