{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Ecully",
      "state": "",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70736",
      "recalling_firm": "In2Bones, SAS",
      "address_1": "28 Chemin Du Petit Bois",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed in the state of TN.",
      "recall_number": "Z-1319-2015",
      "product_description": "DUAFIT(R) PIP 0o CA SIZE 3, REF A60 SP003, STERILE R, Rx only.    Interphalangeal implant.",
      "product_quantity": "15 units",
      "reason_for_recall": "Dimensional non-conformity leading to the impossibility to introduce the implant in the dedicated holder.",
      "recall_initiation_date": "20150309",
      "center_classification_date": "20150325",
      "termination_date": "20160519",
      "report_date": "20150401",
      "code_info": "Batch numbers:  1412021",
      "more_code_info": ""
    }
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}