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FDAMarch 3, 2026device

ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

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

10007916419710088483805905400884838054202

Recall history

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

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