{
  "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-0718-2022",
      "product_description": "COVID-19 IgG/IGM Antibody Test For Detection of COVID-19  IgG and IgM antibodies Catalog No: I-111",
      "product_quantity": "33,955 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-111 Lot Numbers: All Lots due to not having an authorized Emergency Use Authorization (EUA)"
    }
  ]
}