Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Allura Xper FD10 and FD20. X-ray Imaging System. Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to The bolts supporting the FlexMove Carriage may become...
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 NEDERLAND B.V. directly.
Affected Products
Allura Xper FD10 and FD20. X-ray Imaging System.
Quantity: 648 units
Why Was This Recalled?
The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear in the suspension rail of the FlexMove Carriage.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. has 154 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report