{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87936",
      "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": "U.S. Nationwide distribution in the states of MN and OK.    O.U.S.: None",
      "recall_number": "Z-1944-2021",
      "product_description": "FilmArray Pneumonia Panel (Penumo) REF RFIT-ASY-0144",
      "product_quantity": "9 kits (U.S. only)",
      "reason_for_recall": "Elevated rates of false positive/false negative and control failures while using the Pneumonia Panel, due to issues identified in the manufacturing process.",
      "recall_initiation_date": "20210416",
      "center_classification_date": "20210624",
      "termination_date": "20240402",
      "report_date": "20210630",
      "code_info": "Part Number:RFIT-ASY-0144  UDI: 00815381020178    Kit Lot#: 0938121  Pouch Lot#: 19T621"
    }
  ]
}