{
  "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": [
    {
      "country": "United States",
      "city": "Salt Lake City",
      "address_1": "79 W 4500 S",
      "reason_for_recall": "The firm has identified that an incorrect instruction for use (IFU) revision was included in the qualitative, multiplexed, nucleic acid-based in vitro diagnostic test kit.",
      "address_2": "Ste 14",
      "product_quantity": "92 kits",
      "code_info": "Lot No./Expiration Date  457117D/2018-10-17  416118D/2019-03-15  439218D/2019-06-12  439318D/2019-07-18  454218D/2019-08-21  454318D/2019-08-22  455518D/2019-08-23  458118D/2019-09-18  458218D/2019-09-19  458018D/2019-09-20  464018D/2019-10-02  425719D/2020-05-30  462819D/2020-06-10",
      "center_classification_date": "20200305",
      "distribution_pattern": "US: UT, MD, GA, CO, OH, TX,  OUS: None",
      "state": "UT",
      "product_description": "FilmArray NGDS Warrior Panel, Ref: NGDS-ASY-0007, UDI: (01)00851458005136, IVD, Rx Only",
      "report_date": "20200311",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Biofire Defense",
      "recall_number": "Z-1448-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84887",
      "termination_date": "20201030",
      "recall_initiation_date": "20190820",
      "postal_code": "84107-2649",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}