{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97870",
      "recalling_firm": "BioFire Diagnostics, LLC",
      "address_1": "515 S Colorow Dr",
      "address_2": "N/A",
      "postal_code": "84108-1248",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US:AZ, FL,GA,ID NC, NH, NJ, NY, OR, PA, SC OUS: None",
      "recall_number": "Z-0602-2026",
      "product_description": "BioFire Respiratory Panel 2.1, IVD, REF: 423742 (30 test kit)",
      "product_quantity": "97 Kits (2,910 pouches)",
      "reason_for_recall": "Due to  unintended movement of pouch chemistry,  nucleic acid test may result in elevated risk of false negative results and risk of control failures.",
      "recall_initiation_date": "20251022",
      "center_classification_date": "20251126",
      "report_date": "20251203",
      "code_info": "UDI: 00815381020529 /Lot # 2649724 Expanded Lot#: 1471725",
      "more_code_info": ""
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}