FDAFebruary 14, 2023device

Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F.

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

The hazard

Deep Inspiration Breath Hold (DIBH) functionality may not work as specified when based on a standard-workflow Treatment Template

What to do

FDA enforcement status: Ongoing

Brands named

brainlab agbrainlab

UPCs

04056481143978

Recall history

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

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Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F. — Recall Details · AllClear