{
  "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": "2026-04-15",
    "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": "82101",
      "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": "E-Mail",
      "distribution_pattern": "The products were distributed to the following US states: NH.    The products were distributed to the following foreign countries: Germany",
      "recall_number": "Z-1079-2019",
      "product_description": "iTotal Posterior Stabilized (PS) Knee Replacement System, Catalog Number TPS-111-1111 - 020102",
      "product_quantity": "2",
      "reason_for_recall": "The labeling of the boxes and sterile pouches did not match the contents.",
      "recall_initiation_date": "20190104",
      "center_classification_date": "20190330",
      "termination_date": "20200629",
      "report_date": "20190410",
      "code_info": "Serial Numbers 0434436 and 0434836"
    }
  ]
}