{
  "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": "2026-04-08",
    "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": "79681",
      "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": "US Nationwide and the following countries: Brazil, Singapore, Canada, Australia, Japan, Malaysia, Chile, Netherlands, Trinidad",
      "recall_number": "Z-1470-2018",
      "product_description": "ZMS Intramedullary Fixation Smooth Guide Wire  3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-037-00",
      "product_quantity": "19483 total products",
      "reason_for_recall": "Potential failure of sterile packaging seal.",
      "recall_initiation_date": "20180326",
      "center_classification_date": "20180420",
      "termination_date": "20201118",
      "report_date": "20180502",
      "code_info": "Lot Numbers:   63662549  63668704  63696974  63709171  63721377  63731176  63764550  63771164  63781920  63803595  63812302  63817719  63826242"
    }
  ]
}