{
  "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": {
      "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": "83962",
      "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": "Letter",
      "distribution_pattern": "Distributed nationwide.",
      "recall_number": "Z-0331-2020",
      "product_description": "NCB Straight Narrow Plate, various sizes, Item Nos. 0202267008  0202267010  0202267012  0202267014  0202267016  0202267018",
      "product_quantity": "5,459,583 total devices",
      "reason_for_recall": "Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).",
      "recall_initiation_date": "20191010",
      "center_classification_date": "20191107",
      "termination_date": "20200519",
      "report_date": "20191113",
      "code_info": "All products manufactured prior to January 2014."
    }
  ]
}