FDAJuly 18, 2019device

IGuide System, software versions: 2.2.0, 2.2.1, 2.2.2 Product Usage: Linear Accelerator. The intended use of the device is the control of accurate 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

Sometimes, although the HexaPOD has reached the target position, the Constant Correlation Check (CCC) can be too sensitive and iGUIDE may incorrectly demand a verification scan.

What to do

FDA enforcement status: Terminated

Brands named

medical intelligence medizintechnikmedicalmedical intelligence

UPCs

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Recall history

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

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