{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Tuusula",
      "state": "",
      "country": "Finland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95017",
      "recalling_firm": "Palodex Group Oy",
      "address_1": "Nahkelantie 160",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide-Worldwide",
      "recall_number": "Z-2413-2024",
      "product_description": "Orthopantomograph OP300 dental computed tomography x-ray system.    The X-ray device produces conventional 2D X-ray images and Xray  projection images for the reconstruction of a 3D view. The device is operated and  used by qualified healthcare professionals.",
      "product_quantity": "103",
      "reason_for_recall": "It was noticed in production on 28.10.2021, that the final testing database gives a pass result for Pan ADC repeatability test even when the test result is not within  the set acceptance criteria (repeatability within 4%).",
      "recall_initiation_date": "20211028",
      "center_classification_date": "20240812",
      "report_date": "20240821",
      "code_info": "DI: 06430035872725, 06430035872732, 06430035872749, 06430035872756, 06430035872763, 06430035872770",
      "more_code_info": ""
    }
  ]
}