FDASeptember 14, 2021device

Elekta Monaco - Product Usage: used to make treatment plans for patients with prescriptions for external beam radiation therapy.

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

The hazard

Contour changes can be saved on an unintended image set. In addition, these contour edits do not cause the dose to be frozen on the plans associated with that image set.

What to do

FDA enforcement status: Ongoing

Brands named

elekta

UPCs

0085816400219000858164002268

Recall history

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

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