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.
The internal configuration of the electrometers and the Real-Time control boards of the Dekimo Scanning Controller is not checked before each patient treatment.
Ion Beam Applications S.A. recalls their Proteus 235 proton therapy systems because the electrometers and control boards aren't checked before each patient treatment. This could lead to inaccurate radiation delivery during cancer treatments.
The system's electrometers and real-time control boards aren't verified before each patient treatment. This could cause inaccurate radiation delivery during cancer treatments, potentially affecting treatment outcomes.
Patients receiving proton therapy at facilities using the Proteus 235 system are most at risk. Healthcare providers who operate these systems may also be affected.
The Proteus 235 system with model numbers PTS-9.4.X or PTS-10.0.1.1 is recalled. It's used for proton therapy in medical facilities treating cancer patients.
Reach out to Ion Beam Applications S.A. for specific guidance on the recall process.
The recall states that the electrometers and control boards aren't checked before each patient treatment, which could affect treatment accuracy. However, the exact risk level isn't specified in the notice.
The Proteus 235 system with model numbers PTS-9.4.X or PTS-10.0.1.1 is recalled and used for proton therapy in medical facilities.
The recall notice doesn't specify a remedy, so contact Ion Beam Applications S.A. directly for instructions.
We’ve drafted a message you can send Ion Beam Applications S.A. to request your refund or repair — edit it as you like.
Subject: Recall Z-0943-2018 — Ion Beam Applications S.A. Ion Beam Applications S.A. Hello, I own a Ion Beam Applications S.A. that is covered by recall Z-0943-2018 from Ion Beam Applications S.A.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
