FDA recall Z-2109-2018

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

Product

12C (AdaPTinsight) Affected component: AdaPTinsight software Product Usage: 12C is used with a charged particle or photon radiation therapy system for localization of the patient position with respect to the therapy equipment and to provide correction feedback to the radiation therapy system.

Reason for recall

IBA is initiating this recall to address an issue identified with AdaPTinsight software and to reduce risk related to this problem.

Distribution

Worldwide Distribution - US Nationwide in the states of LA, TX, Italy, Sweden and France. Each country's National Competent Authorities were notified of the firm's Field Safety Notice.

Key facts

Status
Terminated
Initiation date
2016-10-28
Report date
2018-06-13
Termination date
2019-08-09
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-2109-2018