Every recall we track for Ion Beam Applications S.A. — 22 in all — plus the complaints and injury reports the public filed about them.
IBA recalls PROTEUS 235 proton therapy systems where safety checks may fail if external gating devices are disconnected. Affected units have specific serial numbers. Contact IBA for details.
Ion Beam Applications recalls PROTEUS 235 proton therapy systems due to temporary collision detection deactivation. Affected units may require repair to prevent safety risks during patient treatment.
Ion Beam Applications recalls specific versions of their Proton Therapy System software due to potential safety parameter deactivation during clinical use. Affected units include ProteusPLUS and ProteusONE software versions PTS-8 through PTS-12.
Ion Beam Applications recalls PROTEUS 23:5 proton therapy systems with C230 accelerator control units that may cause irradiation if critical parameters are outside tolerances. Affected units have specific serial numbers and versions.
Ion Beam Applications recalls specific proton therapy systems due to risk of safety parameters being out of tolerance during irradiation. Affected models include PROTEUS 235, PTS-10, PTS-11, and PTS-12 versions. No remedy is specified in the recall notice.
IBA recalls PROTEUS 235 proton therapy systems with specific versions due to risk of patient crushing during positioning. Affected units have unique serial numbers and software versions.
Ion Beam Applications recalls Proteus235 Proton Therapy System due to potential incorrect radiation dose delivery. Affected units have specific serial numbers and were sold in US/EU. Contact for remedy.
Ion Beam Applications recalls ProteusPLUS and ProteusONE proton therapy systems due to potential risk of incorrect beam range after resuming treatment pauses. This could lead to unintended radiation delivery to patients.
Ion Beam Applications recalls Proteus 235 software versions before PTS-8.7.2 due to potential patient treatment errors from software conflicts between clinical and test environments.
Ion Beam Applications recalls Proteus 235 proton therapy systems due to misleading disconnect messages that may cause incorrect patient treatment. Affected units were sold with specific patents and software versions.
Ion Beam Applications recalls Proteus 235-Proton Therapy Systems with specific serial numbers due to risk of incorrect radiation delivery if trigger input is forgotten during treatment. Affected units include PAT.107 through SAT.133 across multiple regions.
Ion Beam Applications S.A. recalls Proteus 235 proton therapy systems due to inability to load treatment plans after abortion. Affected units have specific serial numbers from May 2019 (US) and October 2019 (EU).
Ion Beam Applications recalls Proteus 235 proton therapy systems where user signatures longer than 10 characters prevent resuming aborted treatments. This medical device affects specific models manufactured between May and November 2019.
Ion Beam Applications S.A. recalls Proteus 235 proton therapy systems due to risk of Compact Gantry Rolling Floor detachment. Affected models include Proteus Plus and Proteus ONE. Consumers should contact the manufacturer for details.
Ion Beam Applications recalls Proteus 235 proton therapy devices due to risk of patient or user injury from improper nozzle alignment during treatment. Affected units may cause crushing or mistreatment if apertures aren't correctly positioned.
Ion Beam Applications S.A. recalls Proteus 235 proton beam devices with specific versions and serial numbers due to risk of incorrect patient positioning during radiation treatment. Affected units may require correction to prevent treatment errors.
Ion Beam Applications recalls Proteus 235, ProteusPLUS, and Proteus ONE proton therapy devices with PTS-7.X.X or PTS-8.X.X software versions. Switching treatment modes may cause under-irradiation or delayed patient treatment with extra X-ray exposure.
Ion Beam Applications recalls Proteus 235 proton therapy systems due to risk of improper accessory insertion causing system operation without proper safety. Affected units may need verification and action.
Ion Beam Applications recalls Proteus 235 proton therapy systems due to potential patient misalignment during multi-isocenter treatments. This medical device is used for cancer treatment. Affected units may require correction to ensure safe radiation delivery.
Ion Beam Applications S.A. recalls Proteus 235 proton therapy systems due to unverified electrometer configuration before patient treatments. This could affect treatment accuracy and safety for cancer patients.
Ion Beam Applications S.A. recalls Proteus 235 graphite block 8 due to incorrect screw hole depth. This may cause malfunction in normal use. No remedy specified.
