{
  "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": "2026-06-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98776",
      "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": "Worldwide - US Nationwide distribution in the states of TX, NC, UT, MD and the countries of France, Italy, Germany, Spain, Belgium, Switzerland, United Kingdom, Netherlands, Poland, Austria, India, Finland, Czech Republic, Egypt, Lebanon, Morocco, Slovenia, Romania, \tDominican Republic, Serbia.",
      "recall_number": "Z-2067-2026",
      "product_description": "BioFire Joint Infection (JI) Panel  REF: RFIT-ASY-0138, 30 test Kit.",
      "product_quantity": "106 kits (3,180 test)",
      "reason_for_recall": "Contamination to in-vitro diagnostic test   may result in false positives.",
      "recall_initiation_date": "20260422",
      "center_classification_date": "20260506",
      "report_date": "20260513",
      "code_info": "Lot #s:0883425,0878825/DI: 00815381020192",
      "more_code_info": ""
    }
  ]
}