{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Holly Hill",
      "state": "FL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90381",
      "recalling_firm": "North American Diagnostics",
      "address_1": "618 Ridgewood Ave",
      "address_2": "N/A",
      "postal_code": "32117-3604",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of  FL, LA, NV, CA, CO, AZ, CT, OH. IL, NY, DC, MD, PA, and the countries of Zambia, Austria, Canada, UAE, Bangladesh.",
      "recall_number": "Z-1401-2022",
      "product_description": "SARS CoV 2 rapid antigen test kits packaged under the following brands:  Oral Rapid Test, Oral Rapid Antigen Test, SML LDT Kits, SML Brand Finished Kits, SML Brand BT Test Kits, SML Brand BT Antigen Test Kit LDT",
      "product_quantity": "122,366 units",
      "reason_for_recall": "Various brands of SARS CoV  2 Antigen Rapid Test kits were offered for sale and distribution to consumers in the United States without marketing approval, clearance, or authorization from FDA.",
      "recall_initiation_date": "20220615",
      "center_classification_date": "20220729",
      "report_date": "20220810",
      "code_info": "Lot:  FLUSA 1020-1, Batches 8, 10, and 12"
    }
  ]
}