{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Buffalo",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71636",
      "recalling_firm": "Ivoclar Vivadent, Inc.",
      "address_1": "175 Pineview Dr",
      "address_2": "N/A",
      "postal_code": "14228-2231",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution in the states of: PA, IN, IA and SC.",
      "recall_number": "Z-2265-2015",
      "product_description": "IPS Empress Universal Glaze Spray 270 mL, Product Code/Model/Catalog Number 609432AN, Rx only.   Porcelain glaze spray used in the fabrication of dental restorations",
      "product_quantity": "Domestic: 27 units",
      "reason_for_recall": "Complaints were received of coarse particles in the glazed surface of IPS e.max Ceram restorations. A basic component of the glass contains a higher number of large grain sizes than usual.",
      "recall_initiation_date": "20150709",
      "center_classification_date": "20150727",
      "termination_date": "20160527",
      "report_date": "20150805",
      "code_info": "Batch U15124"
    }
  ]
}