Recall StatusTerminated
Date Initiated2010-03-23
Date Terminated2012-02-24
Product Quantity218 units
Reason for Recall
Due to software Issue, an error occurs when performing cone planning using MRI, which may result in the patient receiving a higher radiation dose than expected, potentially to healthy tissue.
Firm Action
Varian sent Urgent Medical Device Correction letters on March 23, 2010, by Federal Express to all customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to run test cases or otherwise determine whether the MR images that they receive have the 'Series Date' parameter populated.
Customers should contact their MR system manufacturer to get a confirmation that the 'Series Date' field is populated.
Customers were instructed to confirm by visual inspection that the fusion results are loaded appropriately in Cone Planning before starting to create or edit a plan.
For questions regarding this recall contact your local Varian Customer Support Distirct or Regional Manager.
Phone: USA and Canada - 1-888-VARIANS (888-827-4265)
Europe -+41 41 749 8844
E-mail: North America:
[email protected]
Australia/New Zealand:
[email protected]
Europe:
[email protected]
South East Asia:
[email protected]
China/Asia:
[email protected]
Japan:
[email protected]
Latin America:
[email protected]
Internet: Oncology Systems customer site - www.myvarian.com
Varian Medical System public site - www.varian.com
Distribution Pattern
Worldwide distribution - USA nationwide and the countries of Australia, Brazil, Canada, Chile, Colombia, Georgia, Germany, Hong Kong, India, Ireland, Japan, Macau, Malaysia, Russia, Singapore, Spain, Sri Lanka, and Taiwan
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.