FDAMarch 21, 2017device

Proteus 235, Proton Therapy System

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

The hazard

In specific circumstances, the user is able to restart an aborted irradiation without having to select the correct partial irradiation data.

What to do

FDA enforcement status: Terminated

Brands named

ion beam applicationsionion beam

Recall history

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

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