{
  "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": [
    {
      "status": "Terminated",
      "city": "Bedford",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69867",
      "recalling_firm": "ConforMIS, Inc.",
      "address_1": "28 Crosby Dr",
      "address_2": "N/A",
      "postal_code": "01730-1402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed to IN.",
      "recall_number": "Z-0581-2015",
      "product_description": "Conformis iTotal CR G2 Knee Replacement System  Catalog/Model #: M57250600010    Intended for use as a total knee replacement in patients with knee joint pain and disability.",
      "product_quantity": "1 unit",
      "reason_for_recall": "Incorrect serial number of tibial inserts packaged in tray may result in inserts not fitting",
      "recall_initiation_date": "20141119",
      "center_classification_date": "20141210",
      "termination_date": "20151008",
      "report_date": "20141217",
      "code_info": "Serial Number:  0340552"
    }
  ]
}