FDA recall record

Varian Medical Systems Eclipse Treatment Planning System version 13.MR2 [13.06.31 with Smart recall — FDA Z-0990-2017

Modifications in version 13.6MR2 for Contouring, SmartAdapt, and SmartSegmentation workspaces resulted in contours not being saved consistently in…

Class IIclassification
Z-0990-2017official record ID
Jan 18, 2017report date

Recall record at a glance

Official recordZ-0990-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmVarian Medical Systems, Inc.
Report dateJan 18, 2017
Recall initiation dateDec 2, 2016
Quantity42 devices are affected
LocationPalo Alto, CA, United States

Official product description

Eclipse Treatment Planning System version 13.MR2 [13.06.31 with Smart Segmentation Knowledge Based Contouring version 2.3 [2.3.12] Radiology: The Eclipse Treatment Planning System (Eclipse TPS) is used to plan radiotherapy treatments for patients with malignant or benign diseases. Eclipse TPS is used to plan external beam irradiation with photon, electron and proton beams, as well as for internal irradiation (brachytherapy) treatments.

Why the product was recalled

Modifications in version 13.6MR2 for Contouring, SmartAdapt, and SmartSegmentation workspaces resulted in contours not being saved consistently in Eclipse. Treatment Planning System. The issue only occurs if certain conditions are fulfilled.

Distribution information

US Distribution to the states of : NJ, TN. OR and FL.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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