FDA recall Z-0289-2018

Accuray Incorporated · Class II · device

Product

TomoHDA(R) System, Model Number 1018286 Product Usage: The TomoTherapy treatment system is intended to be used as an integrated system for t he planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of radiation to vital healthy tissues. The megavoltage x-ray radiation is delivered in a rotational, non-rotational, modulated (IMRT), or non- modulated (non-IMRT/3 dimensional conformal) format in accordance with the physicians prescribed and approved plan.

Reason for recall

Uncontrolled couch Z-axis movement (descent)

Distribution

Worldwide Distribution

Key facts

Status
Terminated
Initiation date
2017-11-17
Report date
2018-01-03
Termination date
2021-07-25
Voluntary/Mandated
Voluntary: Firm initiated
Location
Madison, WI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0289-2018