{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Albany",
      "state": "OR",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "89152",
      "recalling_firm": "Dental Alliance Holdings LLC",
      "address_1": "812 Water Ave Ne",
      "address_2": "",
      "postal_code": "97321-3074",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed nationwide with the United States",
      "recall_number": "D-0456-2022",
      "product_description": "CTx26 Kit, contains three tubes of CariFree CTx4 Gel 5000, 1.1% Neutral Sodium Fluoride Mint, 2 oz (57 g) Rx only NDC: 61578-205-01 Manufactured by Oral BioTech Albany, Oregon 97321 and two bottles of CariFree CTx3 Rinse, Mint Anticavity Rinse, 16 fl oz. bottle an two boxes of 4fl.oz. Carifree CTx4 Treatment Rinse.",
      "product_quantity": "225 single tube of lot 31217 and 99 single tube of 312108",
      "reason_for_recall": "Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.",
      "recall_initiation_date": "20211203",
      "center_classification_date": "20220126",
      "termination_date": "20220811",
      "report_date": "20220202",
      "code_info": "Lot#: 312107, 312108 Exp. Date 06/22;  (contains recalled CariFree CTx4 5000 gel tube lot 142017)",
      "more_code_info": ""
    }
  ]
}