{
  "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": "Nantong",
      "state": "",
      "country": "China",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90602",
      "recalling_firm": "Haimen Shengbang Laboratory Equipment Co. Ltd.",
      "address_1": "D, Sanhe",
      "address_2": "No. 50 Xue Qian Road; Sanhezhen Haimen",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of CA, FL, IL & NY. The country of China.",
      "recall_number": "Z-1398-2022",
      "product_description": "HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated Type",
      "product_quantity": "8,710,600total units",
      "reason_for_recall": "Distributed VTM outside of VTM Guidance and without clearance.",
      "recall_initiation_date": "20220712",
      "center_classification_date": "20220808",
      "report_date": "20220817",
      "code_info": "No UDI. All lots distributed in the US.",
      "more_code_info": ""
    }
  ]
}