{
  "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": {
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86550",
      "recalling_firm": "Quidel Corporation",
      "address_1": "10165 McKellar Ct",
      "address_2": "",
      "postal_code": "92121-4201",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "U.S.: AL, AR, AZ, CA, FL, GA, IN, LA, MO, MS, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, and WY",
      "recall_number": "Z-0428-2021",
      "product_description": "QUIDEL Sofia SARS Antigen FIA  IVD  REF 20374",
      "product_quantity": "8,628 kits",
      "reason_for_recall": "Due to false positive results.",
      "recall_initiation_date": "20200925",
      "center_classification_date": "20201106",
      "termination_date": "20240918",
      "report_date": "20201118",
      "code_info": "Model Number 20374  Lot Number: 706142  UPC A GTIN-12: 0 14613 33908 2  Cassettes: 168365 through 166817",
      "more_code_info": ""
    }
  ]
}