Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Azurion 7 B20 System Model Numbers: (1)722068 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to Under certain conditions, the table may move unexpectedly...
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 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; Software Version Number - All versions: R1.X, R2.X, R3.X
Quantity: 1503 units (326 US, 1177 OUS)
Why Was This Recalled?
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
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