{
  "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": "2026-07-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Cambridge",
      "address_1": "150 2nd St",
      "reason_for_recall": "Identified potential false positive MSI-H on the test reports provided to the physicians.",
      "address_2": "",
      "product_quantity": "8 reports",
      "code_info": "Model/Lot/Serial Number:  QRF150009.01 , QRF150228.01 , QRF150108.01 , QRF149795.01,  QRF150117.01 , QRF150247.01 , QRF149634.01 , QRF128938.01",
      "center_classification_date": "20191122",
      "distribution_pattern": "MA, NC,IN, OH, GA",
      "state": "MA",
      "product_description": "FoundationOne CDx test report",
      "report_date": "20191204",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Foundation Medicine, Inc.",
      "recall_number": "Z-0535-2020",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "83729",
      "termination_date": "20210719",
      "more_code_info": "",
      "recall_initiation_date": "20190808",
      "postal_code": "02141-2115",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}