{
  "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-1468-2018",
      "product_description": "Zimmer Natural Nail System Tear Drop Guide Wire  2.4 mm Diameter, 70 cm length; Item Number: 47-2490-098-01",
      "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:   63733044  63748390  63748391  77006546  77006547  77006548"
    }
  ]
}