FDAJuly 8, 2024device

IBA Proton Therapy System - PROTEUS 235 ProteusPLUS and ProteusONE Software versions: PTS-8 versions, PTS-10 versions, PTS-11 versions, and PTS-12 versions

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

The hazard

Safety Parameters Verification Mechanisms can be deactivated in clinical runtime

What to do

FDA enforcement status: Ongoing

Brands named

ion beam applicationsionion beam

UPCs

05404013801138

Recall history

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

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IBA Proton Therapy System - PROTEUS 235 ProteusPLUS and ProteusONE Software versions: PTS-8 versions, PTS-10 versions, PTS-11 versions, and PTS-12 versions — Recall Details · AllClear