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FDAMarch 3, 2026device

Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);

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

The hazard

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

00884838085282008848380992100088483811673300884838103276

Recall history

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

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