{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Kirkland",
      "state": "WA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91863",
      "recalling_firm": "AGILENT TECHNOLOGIES INC./US",
      "address_1": "550 Kirkland Way, Suite",
      "address_2": "N/A",
      "postal_code": "98033",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the states of CA, GA, IN, NJ, and TX.  O.U.S.: None",
      "recall_number": "Z-1358-2023",
      "product_description": "Agilent Resolution ctDx FIRST Sample Collection Kit, 500032",
      "product_quantity": "560 kits",
      "reason_for_recall": "Distributed sample collection kit with an unapproved instruction for use.",
      "recall_initiation_date": "20230217",
      "center_classification_date": "20230411",
      "report_date": "20230419",
      "code_info": "Model/Part Number: 50032 UDI Code: N/A, single site PMA Lot Numbers: 23-0139 23-0140 23-0142 23-0143 23-0159"
    }
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}