FDA recall record

Elekta Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation therapy recall — FDA Z-0987-2017

Cross profile for Varian 60 degree wedge shows "horns."

Class IIclassification
Z-0987-2017official record ID
Jan 18, 2017report date

Recall record at a glance

Official recordZ-0987-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmElekta, Inc.
Report dateJan 18, 2017
Recall initiation dateDec 23, 2016
Quantity433
LocationAtlanta, GA, United States

Official product description

Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation therapy planning software designed to analyze and plan radiation treatment is three dimensions for the purpose of treating patients with cancer.

Why the product was recalled

Cross profile for Varian 60 degree wedge shows "horns."

Distribution information

Worldwide Distribution - US Nationwide in the states of AL, CA, DC, NE, NY, ND, OR, PA, RI, SC, TX, and the countries of Angola, Argentina, Armenia, Australia, Austria, Barbados, Belarus, Brazil, Bulgaria, Canada, China Columbia, Curacao, Czech Republic, Denmark, Finland, France, Germany, Greece, Honduras, Hungary, Iceland, India, Indonesia, Ireland, Italy, Japan, Kazakhstan, Kenya, Malaysia, Netherlands, Norway, Oman, Peru, Poland, Portugal, Romania, Russia, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Kingdom, Yemen, Zambia.

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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