{
  "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": "Clearwater",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91074",
      "recalling_firm": "Endo-Therapeutics, Inc.",
      "address_1": "15201 Roosevelt Blvd Ste 104",
      "address_2": "N/A",
      "postal_code": "33760-3559",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to Florida and Pennsylvania",
      "recall_number": "Z-0270-2023",
      "product_description": "eSuction Small Cavity, Model ET2005",
      "product_quantity": "28 devices",
      "reason_for_recall": "Improper device regulatory classification",
      "recall_initiation_date": "20221024",
      "center_classification_date": "20221118",
      "termination_date": "20240124",
      "report_date": "20221130",
      "code_info": "Model Number: ET2005; UDI-DI: 00816207021393; Lot Numbers: 447037, 447204"
    }
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}