Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to The motorized longitudinal movement of the FlexArm stand...
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 Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;
Quantity: 172 units
Why Was This Recalled?
The motorized longitudinal movement of the FlexArm stand may be inconsistent (not smooth) and eventually may become unavailable. This issue is due to grease leakage from the bearings and/or anti-corrosion oil applied on the bearings, because of which the lubrication on the ceiling rail may be excessive, reducing the friction between the rails and the friction wheel. Expansion to add additional model.
Where Was This Sold?
This product was distributed to 28 states: AL, AZ, AR, CA, CO, FL, GA, HI, IL, IN, KS, KY, MD, MN, MO, NM, NY, OH, OK, PA, RI, TX, UT, VA, WA, WV, WI, WY
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