Recall
FDAHealthOctober 2, 2025

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;

⚠️ 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.

Is this relevant to me?

Geography
AL, AR, AZ, CA, CO, FL, GA, HI, IL, IN, KS, KY, MD, MN, MO, NM, NY, OH, OK, PA, RI, TX, UT, VA, WA, WI, WV, WY
Source agency
FDA
Category
Health
Published
October 2, 2025

Domestic: AL, AR, AZ, CA, CO, FL, GA, HI, IL, IN, KS, KY, MD, MN, MO, NM, NY, OH, OK, PA, RI, TX, UT, VA, WA, WI, WV, WY; International: Australia, Austria, Belgium, Bulgaria, Canada, Czech Republic, Denmark, Finland, France, Germany, Hong Kong, Iraq, Italy, Japan, Netherlands, Norway, Philippines, Poland, Romania, South Africa, South Korea, Spain, Sweden, Switzerland, Thailand, United Kingdom, Vietnam;

What's affected?

Product
Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;
Lot code
Model Number: 722234;

Additional details

Model Number: 722234;

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 172 units.

View original FDA notice →

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