FDA recall Z-2173-2018

Ion Beam Applications S.A. · Class II · device

Product

Proteus 235 The PTS 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 for recall

IBA is recalling to provide information through a Safety Notice to reduce risk for maintenance technicians during ion source replacement.

Distribution

Units were distributed in the USA, Korea, Germany, France, Czech Republic, Italy, Poland, and Sweden. Each country's national Competent Authorities have been informed.

Key facts

Status
Terminated
Initiation date
2016-08-07
Report date
2018-06-20
Termination date
2020-03-25
Voluntary/Mandated
Voluntary: Firm initiated
Location
Louvain La Neuve, N/A, Belgium

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2173-2018