{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Chartres",
      "state": "N/A",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93315",
      "recalling_firm": "LEONI CIA CABLE SYSTEMS",
      "address_1": "5 avenue Victor Hugo",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of MA, TN.",
      "recall_number": "Z-0399-2024",
      "product_description": "ORION System with software OSS v6.0 and OSS v7.0- An electro-mechanical robotic arm for patient positioning in Radiation Therapy, Radiology, or Radiology image-guided treatment environment.  Part Number: 1SOPT00009",
      "product_quantity": "3 units",
      "reason_for_recall": "Users of the patient positioning system ORION System can be faced with a sudden short-term acceleration or with an unintended short-distance movement when the movements are again allowed after an unforeseen interruption signal of motion may result in a collision of the patient with another stationary component of the treatment room.",
      "recall_initiation_date": "20231006",
      "center_classification_date": "20231121",
      "report_date": "20231129",
      "code_info": "UDI-DI:(01)03700383510079 SN 100000004639 SN 100000004698 SN 100000004695",
      "more_code_info": ""
    }
  ]
}