FDAAugust 23, 2019device

Monaco Radiation Treatment Planning System (RTP) System

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

The hazard

Monaco is displaying the Anatomy and Beam shift direction incorrectly on the Monaco Scan and Setup Reference Report and is DICOM exporting incorrect (Anatomy/Beam) shift directions.

What to do

FDA enforcement status: Terminated

Brands named

elekta

UPCs

0085816400224400858164002268

Recall history

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

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