FDAJune 27, 2018device

Proteus 235, Universal Nozzle with snout 300x400; PBS dedicated nozzle with snout XL Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed sma...

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

The hazard

Gantry rotation or proton irradiation can be allowed even if apertures or accessories are not correctly positioned in snout 300x400 or snout XL. This can lead to risk of crushing for patient and/or user, and risk of mistreatment for the patient.

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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