FDAMay 12, 2016device

iGUIDE System, for patient positioning, with assistance of a 30 Tracking System in a radiotherapy environment.

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

The hazard

If by mistake the initial pre-treatment imaging was performed BEFORE the HexaPOD was moved to the DRIVE (*START) position, iGUIDE offers the possibility to branch into a specific catch-up workflow, which was implemented to use the initial scan data.

What to do

FDA enforcement status: Terminated

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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