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FDAMarch 20, 2023device

Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813

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

The hazard

Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operator's foot and injury

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

00884838085015

Recall history

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

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