FDAJuly 3, 2019device

Monaco RTP System, software versions 5.10 and 5.11, Radiation Treatment Planning System

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

The hazard

When creating 3D plans using either MU or Dose weighting modes, if the user changes the number of fractions, rescales the plan and then changes the wedge angle, the Monitor Units are scaled incorrectly.

What to do

FDA enforcement status: Ongoing

Brands named

elekta

Recall history

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

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