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Terminated

Varian brand 4D Integrated Treatment Console (4DITC) Radiation Therapy, version 8.1 SP2 to 10.0 SP1; Model Number: H51; Reference/PSCA Identifier: CP-03940; Product is manufactured and distributed by Varian Medical Systems Inc., Palo Alto, CA Product Usage: 4D Integrated treatment console is designed to assist the operator of a radiation device in providing accurate treatment set-ups for each patient by monitoring set up parameters and preventing the radiation therapy device from commencing irradiation while any parameter is out of conformance with the treatment plan.

FDA Recall Z-3098-2011 · Posted 2011-08-31

Recall StatusTerminated
Product CodeIYE
Date Initiated2011-06-23
Date Terminated2012-03-15

Reason for Recall

Varian has scheduled for an upgrade of the device from current version to 10.2. There are circumstances in which the 4DITC may be involved in a failure to correctly record treatment history information.

Firm Action

Varian Medical Systems, Inc. sent an "Urgent Medical Device Correction/Urgent Field Safety Notice" letter dated June 23, 2011 to all affected customers. The letter identified the product, problem and recommended user actions to follow. Customers were instructed to notify all appropriate personnel of the correction notice. The letter states that the recalling firm will issue a Customer Technical bulletin to inform users of the mandatory upgrade and related information. For future reference, this document will be posted to the Varian customer support website: http://www.MyVarian.com. Any questions regarding this Product Notification letter, contact Varian Medical Systems Help desk at 1-888-827-4265 for USA and Canada and +41417498844 for Europe.

Root Cause

Software design

Distribution Pattern

Worldwide Distribution - USA (nationwide)

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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