{
  "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": "78167",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in US; Internationally Argentina, Netherlands & Canada",
      "recall_number": "Z-0298-2018",
      "product_description": "COMP 12MM HUM FRAC STEM MACRO, model # 11-113562",
      "product_quantity": "N/A",
      "reason_for_recall": "Possibility that the patient label inside the product box was incorrectly labeled.  The outer box label and actual product are correctly identified but the internal patient label could be incorrect.",
      "recall_initiation_date": "20170605",
      "center_classification_date": "20171229",
      "termination_date": "20180306",
      "report_date": "20180110",
      "code_info": "Lot Number: 529890"
    }
  ]
}