{
  "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": [
    {
      "country": "United States",
      "city": "Buffalo",
      "address_1": "175 Pineview Dr",
      "reason_for_recall": "Ivoclar Vivadent, Inc. is recalling a lot of ExciTE F DSC Dental Adhesive found to produce a blue green discoloration when used in combination with cements.",
      "address_2": "",
      "product_quantity": "63 refill packs (50 single use applications per refill)",
      "code_info": "Product Code 630378AN; Lot Number: R59595; Expiration date of 3 January 2015",
      "center_classification_date": "20131121",
      "distribution_pattern": "US Distribution: including states of PA, WA, WI, NY, LA, TX, NJ, CA, OR, IA, SC, IN, IL, and AZ.",
      "state": "NY",
      "product_description": "ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50     dental adhesive for restorations",
      "report_date": "20131127",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ivoclar Vivadent, Inc.",
      "recall_number": "Z-0376-2014",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "66359",
      "termination_date": "20160527",
      "more_code_info": "",
      "recall_initiation_date": "20130923",
      "postal_code": "14228-2231",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}