{
  "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": {
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    {
      "status": "Ongoing",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94942",
      "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": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of WV, IN, AL and the countries of France, Italia, Spain, Greece, Japan Ltd, Singapore, Chile, Taiwan, Israel, Romania, Ecuador, Serbia.",
      "recall_number": "Z-2683-2024",
      "product_description": "BIOFIRE FILMARRAY Pneumonia Panel plus, REF: RFIT-ASY-0143",
      "product_quantity": "24 Kits",
      "reason_for_recall": "Pneumonia panels have an increased risk of control failures due to an issue in the manufacturing process, which could lead to delayed results for the customer.",
      "recall_initiation_date": "20240610",
      "center_classification_date": "20240816",
      "report_date": "20240828",
      "code_info": "UDI-DI: 00815381020314. Lot/Expiration: 2147723/27-Aug-2024",
      "more_code_info": ""
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}