Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to Potential safety issue with the AD7 and AD7X...
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
Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233
Quantity: 324 units US; 1390 units OUS
Why Was This Recalled?
Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
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