Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0287-2018 — TomoHD(R) System, Model Number 1018283 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 min

U.S. FDA — Device Enforcement · United States · 2017-11-17 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0287-2018
Date of alert: 2017-11-17
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Accuray Incorporated
Product category: device
Product type: Devices

Reported risk: Uncontrolled couch Z-axis movement (descent)

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Related