FDAOctober 19, 2020device

MEVION S250i, MEVION S250; Proton Radiation Treatment System - Product Usage: intended to deliver proton radiation treatment to patients with localized tumors or any other conditions susceptible to treatment by radiation

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

The hazard

Treatment beam information disappears on Treatment Console screen while beam delivery continues potential for harm to a patient could occur

What to do

FDA enforcement status: Terminated

Brands named

mevion medical systemsmevionmevion medical

UPCs

0086436600010000864366000124

Recall history

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

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