{
  "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": "81394",
      "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": "Worldwide - US Nationwide Distribution  Foreign:   CANADA  AUSTRALIA  BRAZIL  CHILE  HONG KONG  JAPAN  MALAYSIA  NETHERLANDS  NICARAGUA  SINGAPORE  TAIWAN",
      "recall_number": "Z-0538-2019",
      "product_description": "Zimmer Natural Nail¿ System - Tear Drop Guide Wire, 3.0 mm Diameter, 100 cm Length  Item Number:  47-2490-097-00    Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.",
      "product_quantity": "57241",
      "reason_for_recall": "Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product's chevron opening compromising product sterility",
      "recall_initiation_date": "20181022",
      "center_classification_date": "20181130",
      "termination_date": "20201230",
      "report_date": "20181212",
      "code_info": "All lots expiring prior to September 30, 2023"
    }
  ]
}