{
  "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": "86873",
      "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": "US Nationwide distribution in the state of MO.",
      "recall_number": "Z-0557-2021",
      "product_description": "MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S",
      "product_quantity": "6 units (US)",
      "reason_for_recall": "Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use",
      "recall_initiation_date": "20201027",
      "center_classification_date": "20201210",
      "termination_date": "20210811",
      "report_date": "20201216",
      "code_info": "Lot Codes: V180077300, Exp Date: 2020/10 and    V200009500, EXp Date: 2022/03"
    }
  ]
}