FDAMay 7, 2015device

Treatment Planning and Delivery System Software version 3.6. ViewRay. Indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The software was failing to determine new patient locations if imaging is not enabled during treatment.

What to do

FDA enforcement status: Terminated

Brands named

viewray

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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