Medical device recalls Moderate risk

Brainlab AG recalls RT Elements are applications for radiation treatment planning for use in stereotactic, conformal, computer planned, Lin…

Recall date
November 5, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0647-2016
FDA classification
Class II
Brand / firm
Brainlab AG
Sold / distributed
Worldwide Distribution - US (nationwide) and Internationally to Australia, Belgium, Brazil, Canada, China, France, Germany, Hong Kong, Ireland, Israel, Italy, Japan, Mexico, Portugal, South Korea, Spain, Switzerland, Turkey and the United Kingdom.

Why it was recalled

Large objects with fine resolution are potentially displayed cropped when imported into Brainlab Brain Metastases 1.0.0.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

RT Elements are applications for radiation treatment planning for use in stereotactic, conformal, computer planned, Linac based radiation treatment of cranial, head and neck, and extracranial lesions. The simulated plan is intended for treatment evaluation for example in tumor board meetings or operating rooms

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