FDA Enforcement Class II Terminated

Proteus 235, Pencil Beam Scanning, PTS-9.4.X, PTS-10.0.1.1 The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam treatment room dedicated to the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation localized to the head and neck.

Recall: Z-0943-2018 · Reported March 21, 2018

Enforcement

Recall Number
Z-0943-2018
Event ID
79229
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Ion Beam Applications S.A.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
March 21, 2018
Initiation Date
November 1, 2017
Classification Date
March 9, 2018
Termination Date
March 29, 2019
Address
Chemin du Cyclotron, 3, Louvain La Neuve, N/A, Belgium

Description

Proteus 235, Pencil Beam Scanning, PTS-9.4.X, PTS-10.0.1.1 The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam treatment room dedicated to the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation localized to the head and neck.

Reason

The internal configuration of the electrometers and the Real-Time control boards of the Dekimo Scanning Controller is not checked before each patient treatment.

Code Info

SBF.101 (EU), SBF.105 (US)

Distribution

Worldwide Distribution: US (nationwide) to: MI only and country of: France.

Quantity

3