{
  "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": "Billerica",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86615",
      "recalling_firm": "Conformis, Inc.",
      "address_1": "600 Technology Park Dr",
      "address_2": "N/A",
      "postal_code": "01821-4154",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "US Distribution in CA.",
      "recall_number": "Z-0475-2021",
      "product_description": "iTotal Hip Replacement System, Model number HAA-050-D020-020102    The Conformis Hip System includes standard hip replacement components as well as the following patient specific components: femoral stem and single use instrumentation.",
      "product_quantity": "2",
      "reason_for_recall": "Incorrect hip components were provided in kits.",
      "recall_initiation_date": "20200921",
      "center_classification_date": "20201120",
      "termination_date": "20230612",
      "report_date": "20201202",
      "code_info": "Serial numbers 0469255, 0469255"
    }
  ]
}