{
  "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": [
    {
      "country": "United States",
      "city": "Cranberry Twp",
      "address_1": "120 Marguerite Dr Ste 301",
      "reason_for_recall": "There is an error in the caddy artwork that misidentifies a specific plate and screw.",
      "address_2": "",
      "product_quantity": "6 units",
      "code_info": "Catalog Number: 2111-0005 Lot: 51464",
      "center_classification_date": "20180515",
      "distribution_pattern": "The products were distributed to the following US states: FL, PA, and VA.",
      "state": "PA",
      "product_description": "Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)",
      "report_date": "20180523",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Epic Extremity, LLC",
      "recall_number": "Z-1874-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79824",
      "termination_date": "20190425",
      "more_code_info": "",
      "recall_initiation_date": "20180320",
      "postal_code": "16066-5007",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}