Ion Beam Applications S.A.: Medical Device Recall in 2018 - (Recall #: Z-0930-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Proteus 235, graphite block 8

Product Classification:

Class II

Date Initiated: October 17, 2017

Date Posted: March 14, 2018

Recall Number: Z-0930-2018

Event ID: 79227

Reason for Recall:

IBA identified incorrect screw holes depth in graphite block 8 with respect to the degrader

Status: Terminated

Product Quantity: 3

Code Information:

PAT.115, SAT.116

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated