{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Cypress",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72395",
      "recalling_firm": "Focus Diagnostics Inc",
      "address_1": "11331 Valley View St",
      "address_2": "N/A",
      "postal_code": "90630-5366",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Non US (worldwide): Czech Republic, Denmark, Germany, Italy, Spain and Colombia",
      "recall_number": "Z-0238-2016",
      "product_description": "Focus Diagnostics Anaplasma Phagocytophilum IFA IgM Test Kit, Model No. IF1450M  in vitro diagnostic.",
      "product_quantity": "38 kits",
      "reason_for_recall": "Focus Diagnostics is recalling the Anaplasma phagocytophilum IFA IgM kit because of the potential increase in invalid results.",
      "recall_initiation_date": "20151002",
      "center_classification_date": "20151106",
      "termination_date": "20160129",
      "report_date": "20151118",
      "code_info": "26341, 27011"
    }
  ]
}