HomeMedical Device recalls
Medium severity

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

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateOctober 02, 2025
ReportedDecember 03, 2025
Recalling firmPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Country / regionNetherlands N/A

Hazard

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.

Affected products

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