{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "L'Union",
      "state": "",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91493",
      "recalling_firm": "TEKNIMED SAS",
      "address_1": "Zone Industrielle Montredone",
      "address_2": "11 Rue D Apollo",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - U.S. Nationwide distribution in the state of MS and the countries of Poland, Lithuania, Spain, Taiwan, South Africa, Israel.",
      "recall_number": "Z-1099-2023",
      "product_description": "HIGH V+ Spinal Cement System REF T040321K",
      "product_quantity": "236 systems",
      "reason_for_recall": "Incorrect expiry date.  Product is labeled with expiry date 2027-02-28.  The correct expiration date is 2025-02-28.",
      "recall_initiation_date": "20221215",
      "center_classification_date": "20230206",
      "report_date": "20230215",
      "code_info": "Model/Part Number: T040321K UDI-DI Code: 03760177043084 Batch Number: 060422382",
      "more_code_info": ""
    }
  ]
}