{
  "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": "Hangzhou",
      "state": "",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89755",
      "recalling_firm": "Acon Biotech (Hangzhou) Co., Ltd.",
      "address_1": "398 Tianmushan Road",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: MD, PA  International Distribution to countries of: Hungary and China.",
      "recall_number": "Z-0945-2022",
      "product_description": "Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing), CE marked",
      "product_quantity": "303,760",
      "reason_for_recall": "Non-EUA authorized, CE marked, SARS-CoV-2 antigen rapid test kits are being recalled from the U.S. market because use may lead to inaccurate test results, including false negative or false positive test results.",
      "recall_initiation_date": "20220109",
      "center_classification_date": "20220415",
      "report_date": "20220427",
      "code_info": "Lots: COV1080201, COV1105014",
      "more_code_info": ""
    }
  ]
}