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I2C (IBA Image-Guided Therapy Console)

Ion Beam Applications SA · Model adaPTinsight · UDI-DI 05404013802012

LHN Prescription
10
510(k) clearances
136
Adverse events (2 deaths)
58
Recalls
27
Facilities

Description

Image-Guided Therapy Console

Recalls

DateFirmReason
2026-02-06Hitachi, Ltd. Radiation Oncology Systems, KashiwanohaSoftware anomaly in the patient positioning system may result in positional discrepancy.
2026-02-06Hitachi, Ltd. Radiation Oncology Systems, KashiwanohaSoftware anomaly in the patient positioning system may result in positional discrepancy.
2026-02-03Ion Beam Applications S.A.It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition, the TSS does not interrupt the
2024-07-10Ion Beam Applications S.A.Temporary deactivation of collision detection for Forte Robotic Patient Positioning System occasionally experiences issues
2024-07-08Ion Beam Applications S.A.Safety Parameters Verification Mechanisms can be deactivated in clinical runtime
2024-05-27Hitachi America, Ltd., Particle Therapy DivisionDuring positioning within the system's 3D to 3D matching mode while transferring CBCT images, when the Float Image Selection button is pressed, it may display CBCT images that are
2024-05-27Hitachi America, Ltd., Particle Therapy DivisionDuring positioning within the system's 3D to 3D matching mode while transferring CBCT images, when the Float Image Selection button is pressed, it may display CBCT images that are
2024-05-27Hitachi America, Ltd., Particle Therapy DivisionDuring positioning within the system's 3D to 3D matching mode while transferring CBCT images, when the Float Image Selection button is pressed, it may display CBCT images that are
2024-05-10Ion Beam Applications S.A.Irradiation is not interrupted when some C230 Accelerator Control Unit critical parameters are outside of the defined tolerances
2024-03-04Ion Beam Applications S.A.There is a risk of mistreatment as irradiation is not prevented when some safety parameters are out of tolerance.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.