PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion 7M20 systems with FlexArm ceiling-mounted system.

Recalling company

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Product

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

Reason

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.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

Oct 2, 2025

Reported

Dec 3, 2025

Distribution

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;

Status

Ongoing

Quantity

172 units

Lot / codes

Model Number: 722234;

Company location

Best, N/A

Recall type

Voluntary: Firm initiated

Recall number

Z-0719-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-0719-2026 in the FDA Enforcement Report. Also see FDA recall press releases.