{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Amherst",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75620",
      "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": "Worldwide Distribution - US Nationwide and the countries of  Canada and Australia",
      "recall_number": "Z-0719-2017",
      "product_description": "Virtual XD Test Pack Heavy/Light Fast Set, 2 x 50 ml, REF #/Product Code 646469, Rx ONLY --     Product Usage:  Dental impression material",
      "product_quantity": "US: 2090 units, Canada: 331 units, Australia: 465 units",
      "reason_for_recall": "The firm received complaints claiming the dental material failed to set up.  As the dental material ages, the set time may increase.",
      "recall_initiation_date": "20161109",
      "center_classification_date": "20161207",
      "termination_date": "20180618",
      "report_date": "20161214",
      "code_info": "Lot No./Expiration Date: TL4095/Jan 15, 2017; TL4094/Jan 15, 2017"
    }
  ]
}