{
  "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": "Suwon",
      "state": "N/A",
      "country": "Korea (the Republic of)",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89527",
      "recalling_firm": "SD Biosensor, Inc.",
      "address_1": "1556 Beon-Gil, Yeongtong",
      "address_2": "C4th & 5th Floor Digital Empire Bldg, 16, Deogyeong-Daero",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide Distribution",
      "recall_number": "Z-0719-2022",
      "product_description": "STANDARD Q COVID-19 Ag Home Test    STANDARD Q COVID-19 Ag Home Test is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2 nucleocapsid antigen present in human nasal sample.",
      "product_quantity": "~400,000 kits",
      "reason_for_recall": "Illegal importation of COVID-19 AG Test kits into the U.S. The COVID-19 Ag Test are not approved, cleared or authorized for distribution within the U.S.",
      "recall_initiation_date": "20220131",
      "center_classification_date": "20220315",
      "report_date": "20220323",
      "code_info": "REF No. Q-NCOV-03G Catalog No.: 09COV130 Lot Number: 59628J1T1 (Potentially 59628J1T1/2)"
    }
  ]
}