{
  "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": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84673",
      "recalling_firm": "Wright Medical Technology, Inc.",
      "address_1": "1023 Cherry Rd",
      "address_2": "N/A",
      "postal_code": "38117-5423",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US",
      "recall_number": "Z-1102-2020",
      "product_description": "WRIGHT EVOLVE Proline Head, Size: +2, OD: 22mm, REF 496H222",
      "product_quantity": "48 devices",
      "reason_for_recall": "Two lots of EVOLVE Modular Radial Head could have the wrong size product in the package.  Both the label and laser marking are incorrect on the affected product.",
      "recall_initiation_date": "20191227",
      "center_classification_date": "20200206",
      "termination_date": "20210723",
      "report_date": "20200212",
      "code_info": "Lot code 1633303"
    }
  ]
}