{
  "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": "2026-06-10",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Gimhae",
      "state": "",
      "country": "Korea (the Republic of)",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98739",
      "recalling_firm": "DFI Co., Ltd.",
      "address_1": "388-25 Gomo-Ro",
      "address_2": "Jillye-Myeon",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.",
      "recall_number": "Z-2087-2026",
      "product_description": "One Step K in vitro diagnostic test    REF: 81A4",
      "product_quantity": "761 units",
      "reason_for_recall": "The devices were distributed without required FDA premarket clearance or approval.",
      "recall_initiation_date": "20260402",
      "center_classification_date": "20260506",
      "report_date": "20260513",
      "code_info": "UDI:08806141302650/ Lot: 241023, 250625, 250905",
      "more_code_info": ""
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}