Ion Beam Applications S.A.: Medical Device Recall in 2017 - (Recall #: Z-1695-2017)

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

Product Classification:

Class II

Date Initiated: March 9, 2017

Date Posted: April 5, 2017

Recall Number: Z-1695-2017

Event ID: 76696

Reason for Recall:

The Proton Therapy System can allow gantry rotation even if the snout is not properly locked.

Status: Terminated

Product Quantity: 8 worldwide, 4 in U.S.

Code Information:

Serial numbers: PAT.000, PAT.001, PAT.003, PAT.006, PAT.108, PAT.111, SAT.119, SAT.120

Distribution Pattern:

Distributed in MA, FL, VA, and TN. China, South Korea, France and Germany

Voluntary or Mandated:

Voluntary: Firm initiated