{
  "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": "Changzhou",
      "state": "N/A",
      "country": "China",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90773",
      "recalling_firm": "Jiangsu Well Biotech Co.,Ltd.",
      "address_1": "No 9 Changyang Rd West",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: CA  (pending firm supplying additional distribution locations/consignee list).  O.U.S.: N/A",
      "recall_number": "Z-0001-2023",
      "product_description": "Jiangsu Well Biotech Co.,Ltd. AND SDI LABS COVID-19 Ag Rapid Test Device - Cat#: CO-02",
      "product_quantity": "620,000 tests",
      "reason_for_recall": "Distribution of COVID-19 Ag Rapid Test kits in the U.S. without an Emergency Use Authorization, or a Pre-Market Approval or Clearance.",
      "recall_initiation_date": "20220809",
      "center_classification_date": "20221007",
      "report_date": "20221019",
      "code_info": "Catalog Number: CO-02 UDI-DI Code: No UDI Codes provided Lot Numbers: 202107192, 202108231, 202109231, 202111082, 202110111, 202201102,"
    }
  ]
}