{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Bedford",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73246",
      "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": "KY",
      "recall_number": "Z-1070-2016",
      "product_description": "Conformis iTotal Cruciate Retaining (CR) Knee Replacement System  Model: TCR-111-1111",
      "product_quantity": "1 unit",
      "reason_for_recall": "Incorrect femoral component distributed",
      "recall_initiation_date": "20160128",
      "center_classification_date": "20160308",
      "termination_date": "20160309",
      "report_date": "20160316",
      "code_info": "Serial Number:0363410  UDI - M572TCR1111111021/$$316073103634108"
    }
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}