{
  "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": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77741",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "OH and PA.",
      "recall_number": "Z-0116-2018",
      "product_description": "ROSA BRAIN 3.0.0",
      "product_quantity": "2 devices",
      "reason_for_recall": "Non-conforming product label.",
      "recall_initiation_date": "20160729",
      "center_classification_date": "20171118",
      "termination_date": "20200616",
      "report_date": "20171129",
      "code_info": "Serial No. BR16017 and  BR16018"
    }
  ]
}