{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Lane Cove West",
      "state": "N/A",
      "country": "Australia",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81967",
      "recalling_firm": "Signature Orthopedics Pty Limited",
      "address_1": "Lane Cove W",
      "address_2": "7 Sirius Rd",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Distribution in the states of FL, NY, and TN",
      "recall_number": "Z-0834-2019",
      "product_description": "Genius Knee Cemented CR Femoral Component    Product Usage:  Knee replacement component",
      "product_quantity": "3",
      "reason_for_recall": "Product mix up",
      "recall_initiation_date": "20181210",
      "center_classification_date": "20190214",
      "termination_date": "20201214",
      "report_date": "20190220",
      "code_info": "UDI # 09348215020330  Device Model # 121-07-3000  Lot # 788F7-1"
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}