{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Englewood",
      "state": "CO",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99504",
      "recalling_firm": "Paragon 28, Inc.",
      "address_1": "14445 Grasslands Dr",
      "address_2": "",
      "postal_code": "80112-7062",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution i the state of MT.",
      "recall_number": "Z-2971-2026",
      "product_description": "Custom Made Device Implant 6123 Navicular Cage Small Right Rev A, Model/Catalog Number 6123S R; foot implant",
      "product_quantity": "1",
      "reason_for_recall": "Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.",
      "recall_initiation_date": "20260710",
      "center_classification_date": "20260814",
      "report_date": "20260826",
      "code_info": "Lot Number AOCIA6123",
      "more_code_info": ""
    }
  ]
}