{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plan-Les-Ouates",
      "state": "",
      "country": "Switzerland",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84219",
      "recalling_firm": "SPINEART SA",
      "address_1": "Chemin Du Pre-Fleuri 3",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US: CA    OUS: Unknowns",
      "recall_number": "Z-0546-2020",
      "product_description": "Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures",
      "product_quantity": "14 pieces distribtued to 1 US Distributor",
      "reason_for_recall": "Inner blister pack label is incorrect and does not match the correct external box label.",
      "recall_initiation_date": "20190205",
      "center_classification_date": "20191122",
      "termination_date": "20210428",
      "report_date": "20191204",
      "code_info": "Model Number: JUT-OX 28 09-S  Lot Number: 4-2899  UDI: (01) 0 7640178 97398 5 (11) 181102 (17) 261101 (10) 4-2899",
      "more_code_info": ""
    }
  ]
}