{
  "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": "Terminated",
      "city": "Utsunomiya",
      "state": "N/A",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91829",
      "recalling_firm": "Mani, Inc. - Kiyohara Facility",
      "address_1": "Park 8-3",
      "address_2": "Kiyoharakogyodanchi;  Kiyoharakogyodanchi; Kiyoharakogyodanchi",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distribution in US - 1 consignee in Missouri",
      "recall_number": "Z-1468-2023",
      "product_description": "Mani Trocar Kit, Model MTK23S and Model MTK25S    There are 3 kits contained in one box, and sterile 1 kit consists of 3 pcs. trocar with the valved cannula and 1 pc. infusion cannula.",
      "product_quantity": "45 kits",
      "reason_for_recall": "A packaging defect may compromise the sterile barrier.",
      "recall_initiation_date": "20230220",
      "center_classification_date": "20230426",
      "termination_date": "20250519",
      "report_date": "20230503",
      "code_info": "UDI-DI: 14546951403956 (Model MTK25S)  Mani Trocar Kit: 1) Model MTK23S, Lot V210028903 (exp. 2024-03) 2) Model MTK25S, Lot V210009900 (exp. 2023-03) 3) Model MTK25S, Lot V210006701 (exp. 2023-04) 4) Model MTK25S, Lot V210009101 (exp. 2023-11) 5) Model MTK25S, Lot V220016001 (exp. 2024-11-08)"
    }
  ]
}