{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "10165 Mckellar Ct",
      "reason_for_recall": "Quidel Corporation has initiated a voluntary recall of specific lots of the Sofia Influenza A+B FIA kits because of false positive results which may lead to misdiagnosis.",
      "address_2": "",
      "product_quantity": "13,090 kits (327,250 tests)",
      "code_info": "Lot # Range: 208228-214385, 707916-708108 (29 lots).",
      "center_classification_date": "20130214",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and internationally to Korea, Norway, Germany, Chile, Hong Kong, Switzerland, Netherlands, Thailand, Japan, China, and the UK",
      "state": "CA",
      "product_description": "Quidel, Sofia Influenza A + B FIA, Kit #20218 (25-Test Kit), in vitro diagnostic.",
      "report_date": "20130220",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Quidel Corporation",
      "recall_number": "Z-0819-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64017",
      "termination_date": "20140131",
      "more_code_info": "",
      "recall_initiation_date": "20121203",
      "postal_code": "92121-4201",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}