Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade Recalled by Philips North America Due to Patient tabletop moved out to the home position...
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 directly.
Affected Products
PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to V4.5.1.41989-Intended to produce cross-sectional images of the body Model Number: 728143
Quantity: 428 units
Why Was This Recalled?
Patient tabletop moved out to the home position during scan initialization, may cause operator/bystander staying by the rear of the table to collide with the moved tabletop and be injured
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America
Philips North America has 107 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report