{
  "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": "2026-06-24",
    "results": {
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  "results": [
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      "status": "Ongoing",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98719",
      "recalling_firm": "BioFire Diagnostics, LLC",
      "address_1": "515 S Colorow Dr",
      "address_2": "",
      "postal_code": "84108-1248",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of MS, TX MN, VA.",
      "recall_number": "Z-2081-2026",
      "product_description": "Biofire Spotfire Respiratory/Sore Throat Panel  REF: 423485",
      "product_quantity": "2400 pouches",
      "reason_for_recall": "Respiratory/sore throat panel  test may result in false negative results and control failures.",
      "recall_initiation_date": "20260401",
      "center_classification_date": "20260506",
      "report_date": "20260513",
      "code_info": "Lot Number: 2215125/UDI: 00815381020390",
      "more_code_info": ""
    }
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}