Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Allura Xper FD20 Biplane system with an ADN7NT patient Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to When Software upgrade 8.1.100 is installed on an...
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
Philips Allura Xper FD20 Biplane system with an ADN7NT patient table. Model Number: 722013, Software Version Number 8.1.100.
Quantity: 1 unit (OUS)
Why Was This Recalled?
When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected movements of the table.
Where Was This Sold?
This product was distributed to 1 state: OK
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