{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Rillieux La Pape",
      "state": "",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84770",
      "recalling_firm": "Medicrea International",
      "address_1": "5389 Route De Strasbourg",
      "address_2": "Vancia",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "OH, VA",
      "recall_number": "Z-1156-2020",
      "product_description": "Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device  Catalog: Number A24200010",
      "product_quantity": "14 units",
      "reason_for_recall": "Inner draw rod, which threads into the cage may potentially be separated from the proximal knob of the inserter",
      "recall_initiation_date": "20191002",
      "center_classification_date": "20200212",
      "termination_date": "20210208",
      "report_date": "20200219",
      "code_info": "Lot Numbers l9B0570; 19B0572",
      "more_code_info": ""
    }
  ]
}