{
  "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": "2026-04-08",
    "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": "77891",
      "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": "Letter",
      "distribution_pattern": "Distribution was nationwide.  Foreign distribution was made to Canada, Bulgaria, Namibia, New Zealand and Germany.  There was no military /government distribution.",
      "recall_number": "Z-3217-2017",
      "product_description": "Ultradent Products, Inc.  Paper Points, Size 45 PN #1558, 200 per container, sterile.     Product Usage:  The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins..",
      "product_quantity": "26 units",
      "reason_for_recall": "The barcode label was placed underneath the sterile barrier and the product was re-wrapped.",
      "recall_initiation_date": "20170804",
      "center_classification_date": "20170926",
      "termination_date": "20180104",
      "report_date": "20171004",
      "code_info": "Lot numbers BDB9Q, BDHWK, BDTBJ, and BDX3F"
    }
  ]
}