{
  "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": "Glendora",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73293",
      "recalling_firm": "Ormco/Sybronendo",
      "address_1": "1332 S Lone Hill Ave",
      "address_2": "N/A",
      "postal_code": "91740-5339",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide and the countries of Canada, Australia, Mexico, Europe, Hong Kong, MY, IN, JP, ID, SG, TH",
      "recall_number": "Z-1083-2016",
      "product_description": "TF Adaptive Gutta Percha Point Size SM3 50pk, Part No. 815-1541    Intended to fill a endontontically obturated root canal treatment",
      "product_quantity": "5,568 units total (2,070 units in US)",
      "reason_for_recall": "Ormco Corporation is recalling the TF Adaptive Gutta Percha Point Size SM3-50pk because the inner generic label is identified as ML3.  The products outer package is identified as SM3 which matches the product inside.",
      "recall_initiation_date": "20160208",
      "center_classification_date": "20160308",
      "termination_date": "20160830",
      "report_date": "20160316",
      "code_info": "GE15011637"
    }
  ]
}