{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Earth City",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84249",
      "recalling_firm": "Young Dental Manufacturing Co, LLC",
      "address_1": "13705 Shoreline Ct E",
      "address_2": "N/A",
      "postal_code": "63045-1202",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of MS, IN, MD, IL, TN, NJ, an ME.",
      "recall_number": "Z-0661-2020",
      "product_description": "Oral-B, Practitioner Series, 5% Sodium Fluoride Varnish, 500 units (40mL/each) - Product Usage: For dentinal hypersensitivity and for the reduction of post-operative sensitivity.",
      "product_quantity": "Batch 84702 - 6500 units; Batch 72766 - 6500 units",
      "reason_for_recall": "Product shelf life may be shorter than that indicated on the label.",
      "recall_initiation_date": "20191030",
      "center_classification_date": "20191209",
      "report_date": "20191218",
      "code_info": "Batch 84702; Batch 72766",
      "more_code_info": ""
    }
  ]
}