FDAMay 16, 2018device

Proteus 235, Version PTS-11.0.1.2 and PTS-11.0.2 Product Usage: A device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.

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

The hazard

Correction vector confirmation message is lost if access point is changed after sending the correction vector. As a result, the patient will be treated in the setup position or treatment position instead of the corrected position.

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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