{
  "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": "Rillieux La Pape",
      "state": "",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84595",
      "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": "Nationwide",
      "recall_number": "Z-0827-2020",
      "product_description": "Medicrea Pass LP Trocar K-wire 01.6mm x 500mm-Nitinol  Product reference : A06010130",
      "product_quantity": "30 units",
      "reason_for_recall": "Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the minimum tolerance axis threaded",
      "recall_initiation_date": "20190916",
      "center_classification_date": "20200118",
      "report_date": "20200129",
      "code_info": "Lot number(s) : 18G0037",
      "more_code_info": ""
    }
  ]
}