{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Nanjing",
      "state": "",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79911",
      "recalling_firm": "Micro-Tech (Nanjing) Co., Ltd.",
      "address_1": "High Tech",
      "address_2": "NO. 10 Gaoke Third Road Nanjing National",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US distribution to one distributor in MI.",
      "recall_number": "Z-1878-2018",
      "product_description": "Trident Endoscopic Ultrasonic Aspiration Needle (FNA)",
      "product_quantity": "40 total",
      "reason_for_recall": "The combination of the firmness of the mass, the potential endoscope and elevator position combined with the force required to penetrate the mass may contribute to the breakage of the needle in the human body, which could cause injury.",
      "recall_initiation_date": "20180312",
      "center_classification_date": "20180515",
      "termination_date": "20180830",
      "report_date": "20180523",
      "code_info": "Identifier EUS-22-0-N  UPN ES34601  M171226172",
      "more_code_info": ""
    }
  ]
}