{
  "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-0457-2022",
      "product_description": "CTx36 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 six boxes of 4fl.oz. Carifree CTx4 Treatment Rinse.",
      "product_quantity": "90 single tubes of 352110 and 315 single tubes of 352111",
      "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 #: 352110, 352111 Exp. Date 06/22;  (contains recalled CariFree CTx4 5000 gel tube lot 142017)",
      "more_code_info": ""
    }
  ]
}