FDAJanuary 26, 2026device

Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

884838085282884838099210884838116733

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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