4D Integrated Treatment Console (4DITC) TrueBeam Linear Accelerator Varian Medical Systems, Palo Alto, CA. The 4DITC is designed to interface to the Varian Clinac Treatment Control System for the purpose of providing verification of treatment parameters, imaging and providing a record of treatment.. The True Beam is a medical linear accelerator which delivers X-ray and electron radiation for sterotactic radiosurgery and therapeutic radiation.
FDA Recall Z-0691-2012 · Posted 2012-01-11
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Recalling FirmVarian Medical Systems, Inc. Oncology Systems
Recall StatusTerminated
Product CodeIYE
Date Initiated2011-12-12
Date Terminated2012-07-26
Product Quantity4875 units
Reason for Recall
Varian has discovered that on 4D Integrated Treatment Console and TrueBeam, the ad-hoc CIAO(Complete Irradiated Area Outline) calculation results in the CIAO generation that is different from the CIAO in RT Chart. The 4DITC algorithm adds dose for the control point at field edge, which should not be added according to the system specifications.
Firm Action
Varian Medical Systems sent a Urgent Medical Device Notice dated December 22, 2011, to all affected customers via certified mail. The letter identified the product the problem and the action needed to be taken by the customer. The Letter will also be distributed to the Varian Sales, Marketing, and Service organizations, informing them of the recall.
***12-20-12, AMENDED INFO ***: An additional letter was sent to consignees on 11/5/12 that Varian identified as also being affected by the recall.***
Canadian account letters were sent by Fed Ex. International Customer Support Managers were sent letters for translation (when necessary) prior to sending to accounts.
All of the information will be posted on the Varian web site and all appropriate personnel in the radiotherapy department should be advised of the content of
this letter. A complete list of affected code numbers is included as well as contact information for Varian Oncology Help Desk. USA and Canada - 888-827-4265.
Root Cause
Device 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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