{
  "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": "Warsaw",
      "address_1": "1800 W Center St",
      "reason_for_recall": "Durability characteristics of reusable instruments were not established",
      "address_2": "",
      "product_quantity": "Greater than 10,000,000 last 10 years",
      "code_info": "All lots in distribution prior to 5/8/17",
      "center_classification_date": "20170531",
      "distribution_pattern": "Nationwide Worldwide",
      "state": "IN",
      "product_description": "Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.",
      "report_date": "20170607",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-2198-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77223",
      "termination_date": "20171201",
      "more_code_info": "",
      "recall_initiation_date": "20170508",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}