FDAApril 15, 2019device

PROBEAT-V, software versions 4.8.1S, and 5.1M Radiation therapy system.

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

The hazard

There is a potential for a discrepant target position when using 3D3D matching mode in PIAS (Positioning Image Analysis System) software installed in the PROBEAT-V, proton therapy systems.

What to do

FDA enforcement status: Terminated

Brands named

hitachi america ltd power systems divisionhitachihitachi america

Recall history

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

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