{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Billerica",
      "address_1": "600 Technology Park Dr",
      "reason_for_recall": "The stage 1 and 2 reamer instruments used to prepare fixation for the cup in the acetabulum had a -1mm interference fit with acetabulum bone. The expected interference fit is -2mm.",
      "address_2": "",
      "product_quantity": "1",
      "code_info": "Serial Number 0424647",
      "center_classification_date": "20190111",
      "distribution_pattern": "The products were distributed to the following US states:  TN.",
      "state": "MA",
      "product_description": "iTotal Hip Replacement System, Total Hip Replacement System, Catalog Number HAA-050-D001-020101",
      "report_date": "20190123",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Conformis, Inc.",
      "recall_number": "Z-0731-2019",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "81723",
      "termination_date": "20200629",
      "more_code_info": "",
      "recall_initiation_date": "20181016",
      "postal_code": "01821-4154",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}