{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Winter Park",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85403",
      "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": "Worldwide distribution - US Nationwide distribution including in the states of  IL, IN, MO,TN, and the country of Denmark.",
      "recall_number": "Z-2005-2020",
      "product_description": "Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: This device is disposable and is packaged and sterilized for single use only. The bag may be used for multiple specimen retraction.",
      "product_quantity": "1550",
      "reason_for_recall": "Genicon is providing updated IFU labeling to users to provide clarity on how to use the device for multiple specimen retrieval.",
      "recall_initiation_date": "20180627",
      "center_classification_date": "20200514",
      "report_date": "20200520",
      "code_info": "Device Model 550-000-000; UDI 00877972005230; Lot I8920/2020-08-29"
    }
  ]
}