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FDAMarch 3, 2026device

Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (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

008848380992340088483811675700884838110564

Recall history

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

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Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only); — Recall Details · AllClear