{
  "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": "South Jordan",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75796",
      "recalling_firm": "Ultradent Products, Inc.",
      "address_1": "505 W 10200 S",
      "address_2": "N/A",
      "postal_code": "84095-3800",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution - US Nationwide",
      "recall_number": "Z-0704-2017",
      "product_description": "UltraSeal XT Plus Clear Refill.  The package contains 4x 1.2 ml UltraSeal XT Plus.    Product Usage:  The UltraSeal XT Plus is used for prophylactic sealing of pits and fissures. It may also be used for micro restorative or initial layer of composite restorations.",
      "product_quantity": "31",
      "reason_for_recall": "There was a labeling error with product, UltraSeal XT Plus Clear Refill, Part Number (PN) 565, Lot Number (Lot) BD79T.  The package was mislabeled as PQ1, PN 641; while the barcode, IFU and products were labeled for UltraSeal XT Plus Clear Refill, PN 565, Lot BD79T.",
      "recall_initiation_date": "20161117",
      "center_classification_date": "20161203",
      "termination_date": "20170605",
      "report_date": "20161214",
      "code_info": "Lot BD79T"
    }
  ]
}