{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Cypress",
      "address_1": "11331 Valley View St",
      "reason_for_recall": "Focus Diagnostics initiated the recall of the certain  Simplexa Flu AlB & RSV Direct assay kits due to  the potential of false positive Flu A, Flu B and RSV signals.",
      "address_2": "",
      "product_quantity": "2,175 kits",
      "code_info": "Model Number MOL2650. Lot Numbers: 24493, 24495, 24535, 24536, 24591, 24603, 24605, 24732, 24773, 24788, 24797, 24807.",
      "center_classification_date": "20140305",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and to countries of:Canada, Sweden, Belgium, Spain, Portugal, Slovenia, and Israel.",
      "state": "CA",
      "product_description": "Simplexa Flu AlB & RSV Direct Assay Kits, intended for use as an aid in the differential diagnosis of influenza A, influenza B, and RSV viral infections in humans and is not intended to detect influenza C. Model Number MOL2650.",
      "report_date": "20140312",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Focus Diagnostics Inc",
      "recall_number": "Z-1144-2014",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "67436",
      "termination_date": "20141101",
      "more_code_info": "",
      "recall_initiation_date": "20140204",
      "postal_code": "90630-5366",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}