{
  "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": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89539",
      "recalling_firm": "Lusys Laboratories, Inc.",
      "address_1": "7220 Trade St Ste 338",
      "address_2": "N/A",
      "postal_code": "92121-2324",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of CA, NC, NV, OH, TN and TX. The countries of Canada, China, and Mexico.  Pending additional information for a complete Consignee Listing",
      "recall_number": "Z-0717-2022",
      "product_description": "Luscient Diagnostics 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114(Nasal Swab Test)",
      "product_quantity": "90,849 kits",
      "reason_for_recall": "COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are not authorized, cleared, or approved for marketing and/or distribution in the U.S.",
      "recall_initiation_date": "20220113",
      "center_classification_date": "20220310",
      "report_date": "20220316",
      "code_info": "Part Number: I-114(N) Lot Numbers:  All Lots due to not having an authorized Emergency Use Authorization (EUA)"
    }
  ]
}