{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Chicago",
      "address_1": "1552 W Carroll Ave",
      "reason_for_recall": "Medacta has registered in its database 3 cases of breakage of the GMK Intramedullary Extension  Rod 100 mm, code 02.07.10.0162.",
      "address_2": "",
      "product_quantity": "1 rod (US); 145 rods (global)",
      "code_info": "Model Number: 02.07.10.0162",
      "center_classification_date": "20141112",
      "distribution_pattern": "Worldwide Distribution - US including OH and Internationally to Australia, Austria, Belgium, France, Germany, Greece, Italy, Japan, Portugal, South Africa, Spain, and Switzerland.",
      "state": "IL",
      "product_description": "GMK Intramedullary Extension Rod 100 mm is a rod to obtain correct leg alignment during total knee replacement.  Rod to obtain correct leg alignment during total knee replacement.",
      "report_date": "20141119",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medacta Usa",
      "recall_number": "Z-0202-2015",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "69493",
      "termination_date": "20150507",
      "more_code_info": "",
      "recall_initiation_date": "20140922",
      "postal_code": "60607-1012",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}