Ion Beam Applications S.A.: Medical Device Recall in 2017 - (Recall #: Z-2672-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Proteus 235 and Proteus ONE proton therapy systems

Product Classification:

Class II

Date Initiated: May 18, 2016

Date Posted: July 12, 2017

Recall Number: Z-2672-2017

Event ID: 77620

Reason for Recall:

Recall is being initiated to address on-site software installations not being performed consistently with IBA standard operating procedures.

Status: Terminated

Product Quantity: 18 worldwide and 10, in the U.S.

Code Information:

Code/Serial Numbers: PAT.003, PAT.006, PAT.107, PAT.108, PAT.109, PAT.110, PAT.111, PAT.112, PAT.113, PAT.114, PAT.115, SAT.116, SAT.117, SAT.119, SAT.120, SAT.122, SAT.123 and SAT.126

Distribution Pattern:

Products distributed to FL, VA, PA, OK, IL, NJ, WA, TN, LA, TX, South Korea, Germany, France, Czech Republic, Italy, Poland, and Sweden

Voluntary or Mandated:

Voluntary: Firm initiated