FDAJune 14, 2021device

Proteus 235- 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

Users may be misled by the popup message displayed by the Proton Therapy System when the Oncology Information System appears disconnected, may cause mistreatment

What to do

FDA enforcement status: Ongoing

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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Proteus 235- designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation — Recall Details · AllClear