FDAJune 30, 2023device

Wireless Foot Switch distributed with Philips Allura Xper and Azurion Interventional Fluoroscopic X-Ray Systems

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

The hazard

Loss of availability of the wireless foot switch during procedures.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

459800772231459800772233459800772261459800772263459800415531459800415532459800415533459800415534459800415535459800415571459800415572459800415573

Recall history

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

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