{
  "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": "Terminated",
      "city": "Ecully",
      "state": "N/A",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87341",
      "recalling_firm": "In2Bones, SAS",
      "address_1": "28 Chemin du petit Bois",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of TN.",
      "recall_number": "Z-1283-2021",
      "product_description": "In2Bones Shannon Percutaneous Burr - Product Usage:  indicated for forefoot mini-invasive and percutaneous surgery.",
      "product_quantity": "60 units",
      "reason_for_recall": "This Field Action is being conducted following identification of manufacturing non-conformity of some batches of Shannon burrs diameter 2.0mm length 20mm, possibly causing the breakage of the burr during use.",
      "recall_initiation_date": "20210209",
      "center_classification_date": "20210319",
      "termination_date": "20240711",
      "report_date": "20210331",
      "code_info": "Model G01 01511, Batches 2009139 and 2001089  Model G01 01512, Batches 2007087 and 2011062",
      "more_code_info": ""
    }
  ]
}