{
  "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": "83760",
      "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": "Visit",
      "distribution_pattern": "Distributed to consignees in MD and NV.",
      "recall_number": "Z-0064-2020",
      "product_description": "iTotal Hip Replacement System, Model HBS-033-0013-020101, Size 13 Hip-Patient Specific Stem Right",
      "product_quantity": "1",
      "reason_for_recall": "Two femoral stems, sizes 13 and 15, were erroneously switched and packed in each other's packaging.",
      "recall_initiation_date": "20190822",
      "center_classification_date": "20191008",
      "termination_date": "20200708",
      "report_date": "20191016",
      "code_info": "0447621"
    }
  ]
}