{
  "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": "Winter Park",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78655",
      "recalling_firm": "Genicon, Inc.",
      "address_1": "6869 Stapoint Ct Ste 112",
      "address_2": "N/A",
      "postal_code": "32792-6603",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed domestically to FL, IL, MI, TN, UT.      Distributed internationally to Dominican Republic, Ireland, Denmark, Spain, Switzerland, United Kingdom.",
      "recall_number": "Z-1076-2018",
      "product_description": "GENICON EZEE Retrieval, sterile, Rx only.",
      "product_quantity": "2,967 units",
      "reason_for_recall": "Plastic handle is breaking off of shaft inhibiting proper removal per Instructions for Use.",
      "recall_initiation_date": "20170719",
      "center_classification_date": "20180316",
      "termination_date": "20200518",
      "report_date": "20180328",
      "code_info": "Catalog No. 550-000-000; Lot No. I8095/2017-11-08, I8162-2018-01-09, I8162/2020-01-09; UDI: 00877972005223."
    }
  ]
}