Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Allura Xper FD20 Ceiling version only Recalled by Philips Electronics North America Corporation Due to Normally, movement of the C-arc is initially stopped...
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
Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.
Quantity: 15 subject to correction and removal
Why Was This Recalled?
Normally, movement of the C-arc is initially stopped by the motor (holding torque) then by the electromagnetic brake, leading to a full stop of the C-arc. Because of improper adjustment and tolerances, when the C-arc is initially stopped in an unbalanced position, the air gap of the brake can become too large, resulting in continued C-arc movement (C-arc is looking for balanced position).
Where Was This Sold?
This product was distributed to 2 states: IN, TN
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