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Terminated

4D Integrated Treatment Console v 8.6 with ARIA RT Chart v8.5, all of 4DITC v 8.3; Varian Medical Systems, Palo Alto, CA Designed to assist the operator of a radiation therapy device in providing the radiation therapy device from commencing irradiation when any parameter is out of conformance with the treatment plan.

FDA Recall Z-3194-2011 · Posted 2011-09-14

Recall StatusTerminated
Product CodeIYE
Date Initiated2011-07-21
Date Terminated2013-08-01
Product Quantity1125

Reason for Recall

The 4D Integrated Treatment Console may erratically fail to load the planned physical wedge accessory without warning or notification when receiving an approved plan from the oncology information system.

Firm Action

Urgent Medical Device Correction/Field Safety Notification letters were sent to all US consignees by Certified Mail on July 21, 2011., as well as Varian Sales, Marketing and Service Organizations. Varian International Customer Support managers will notify international customers by appropriate methods. The letter informed customers of the issue and the corrective action steps. Letters request that all appropriate personnel working in the radiotherapy department be notified of the contents of the letter. A new release version is being created to correct the issue. All sites will be notified when it is available. Questions or concerns should be directed to 1-888-827-4265. Contact information for international customers is also provided as well as a list of all affected serial numbers.

Root Cause

Pending

Distribution Pattern

Worldwide Distribution -- USA, China, Austria, Belgium, Bulgaria, Czech Republic, Denmark, Estonia, Finland, France, Germany, Guadeloupe, Ireland, Italy, Latvia, Lithuania, Martinique, Netherlands, Poland, Portugal, Slovakia, Slovenia, Spain, Sweden, Turkey, United Kingdom, Singapore, Algeria, Bangladesh, Belarus, Egypt, Guam, Hong Kong, India, Indonesia, Iraq, Israel, Kenya, Kuwait, Macau, Malaysia, Philippines, Qatar, Russia, South Africa, South Korea; Taiwan, Thailand, Tunisia, Ukraine, United Arab Emirates, Japan, Brazil, Chile, Columbia, Dominican Republic, Ecuador, Mexico, Peru, Venezuela, New Zealand, and Australia.

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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