{
  "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": "88410",
      "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 : FL, MI, NJ, OH, VA and WI.    O.U.S.: None",
      "recall_number": "Z-2245-2021",
      "product_description": "FilmArray Blood Culture Identification (BCID) Panel    Product Pouch Label:  FilmArray BCID Panel    Part No: RFIT-ASY-0126  Part No: RFIT-ASY-0127",
      "product_quantity": "29 kits",
      "reason_for_recall": "Due to product complaints received for false negative results (dropouts) with blood culture identification panel potential caused by a pouch manufacturing error.",
      "recall_initiation_date": "20210720",
      "center_classification_date": "20210811",
      "termination_date": "20221216",
      "report_date": "20210818",
      "code_info": "Part No: RFIT-ASY-0126 / UDI: 00815381020086;    Part No: RFIT-ASY-0127 / UDI: 00815381020093;    Kit Lot# 0868221;  Pouch Lot# 194Z21;  Batch 003"
    }
  ]
}