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FDANovember 18, 2015device

MEVION S250 Radiation therapy system

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

The hazard

The treatment table positioning belt can slip gear positions, resulting in deviation of patient setup and treatment positions from the time of slippage until the discovery of slippage and the halting of treatment.

What to do

FDA enforcement status: Terminated

Brands named

mevion medical systemsmevionmevion medical

Recall history

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

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