FDAJune 29, 2018device

MEVION S250/MEVION S250i Proton Beam Radiation therapy system Product Usage: Indicated for the delivery of radiation for the treatment of patients with localized tumors or other conditions susceptible to treatment by radiation.

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

The hazard

QFix has advised Mevion Medical Systems that they are identifying unauthorized combinations of QFix Couch Tops with non-QFix devices in clinical use. The kVue Oen Touch latch consists of a precision latch mechanism that can be damaged when used with incompatible (third-party) accessories. This can create unsafe conditions for use and may compromise the subsequent use of any kVue inserts, whether authorized or not. Use of unauthorized or unvalidated inserts may lead to an incorrect patient treatment or physical injury.

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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