Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1271-2014 — MEVION S250, System, Radiation Therapy, Charged-Particle, Medical used for Proton Radiation Therapy Product Usage: Proton Radiation Therapy

U.S. FDA — Device Enforcement · United States · 2014-03-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1271-2014
Date of alert
2014-03-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Mevion Medical Systems, Inc.
Product category
device
Product type
Devices
Reported risk: Geometric positioning error can occur after a rotational correction has been applied to one or more treatment fields
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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