Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to Loss of connectivity between the FlexArm and the...
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 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)
Quantity: 28 systems (9 US, 1 Canada, 18 ROW)
Why Was This Recalled?
Loss of connectivity between the FlexArm and the Table due to a software issue.
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