{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "203853",
      "product_res_number": "Z-0295-2024",
      "event_date_initiated": "2023-09-18",
      "event_date_posted": "2023-11-14",
      "recall_status": "Open, Classified",
      "res_event_number": "93293",
      "product_code": "LHN",
      "k_numbers": [
        "K163500"
      ],
      "product_description": "IBA Proton Therapy System - PROTEUS 235. PTS-11 versions, PTS-12 versions with Orion PPS version OSS6.0. Configured with Orion Patient Positioning System.",
      "code_info": "UDI-DI: (01)05404013801138. \nSerial numbers (US): SAT133, SAT140, SBF113, SBF128, SBF135 & (OUS): SAT125, SAT127, SAT132, SAT136, SBF107, SBF112, SBF117, SBF124, & SBF125.",
      "firm_fei_number": "3000256071",
      "recalling_firm": "Ion Beam Applications S.A.",
      "address_1": "Chemin Du Cyclotron 3 3 chemin du cyclotron",
      "city": "Ottignies-Louvain-La-Neuve",
      "country": "Belgium",
      "additional_info_contact": "Sonia Pinel\n32-25072081",
      "reason_for_recall": "The patient positioning system can perform motions in unexpected directions, creating the potential for crushing of the patient between the patient positioning devices.",
      "root_cause_description": "Device Design",
      "action": "An Urgent Medical Device Correction issued on October 4, 2023 by email or in-person visit. Waiting for the solution to be deployed, IBA requires the user to only request jog translation motions to recover from a collision situation. IBA also recommends the user to post the notice near the device to remind them of this requirement until the software correction can be deployed. IBA provide an updated Urgent Medical Device Correction notification by November 30, 2023 with a target date for deployment of the software solution to your site. Customers are to complete and return the acknowledgement form to IBA. IBA Contact: Sonia Pinel Head of Post Market Vigilance, Email: Vigilance@iba-group.com, Helpdesk: +32 2 507 20 81 (available 24/7).",
      "product_quantity": "5 (US), 9 (OUS)",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of Arkansas, Florida, Kansas, and Virginia and the countries of Belgium, France, India, Italy, Netherlands, Spain, Singapore, and Taiwan.",
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        "device_name": "System, Radiation Therapy, Charged-Particle, Medical",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.5050",
        "device_class": "2"
      }
    }
  ]
}