{
  "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": "Amherst",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79064",
      "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 and Canada",
      "recall_number": "Z-0665-2018",
      "product_description": "Heliomolar Refill 20x0.25g 110/A1, Product code 541501AN, Catalog number 541501",
      "product_quantity": "2,153 units",
      "reason_for_recall": "Complaints were filed claiming the material consistency was too soft and too sticky in comparison to its usual consistency, causing unexpected handling for the user during packing and contouring.",
      "recall_initiation_date": "20170803",
      "center_classification_date": "20180221",
      "termination_date": "20180828",
      "report_date": "20180228",
      "code_info": "Batch: V35109 Exp. date: 01.10.2020; Batch: V40817 Exp. date: 13.11.2020; Batch: V48597 Exp. date: 30.12.2020; Batch: V48938  Exp. date: 31.12.2020 Batch: W12251 Exp. date: 31.03.2021"
    }
  ]
}