FDAAugust 15, 2023device

Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and MultiDiagnost-Eleva systems

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

The hazard

A damaged foot switch may cause instances where no or only intermittent x-ray radiation initiation is possible.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

Recall history

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

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