{
  "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,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Louisville",
      "state": "KY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90639",
      "recalling_firm": "Dental Choice Holding Llc",
      "address_1": "10100 Linn Station Rd",
      "address_2": "N/A",
      "postal_code": "40223-3861",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1494-2022",
      "product_description": "CustMbite, Model Number CBT-SRS-UL",
      "product_quantity": "708",
      "reason_for_recall": "The device was marketed and sold in the US without FDA clearance.",
      "recall_initiation_date": "20220523",
      "center_classification_date": "20220802",
      "report_date": "20220810",
      "code_info": "UDI-DI: N/a Lot codes: SS-J21287-200-1021, SS-K21333-510-1121, SS-B22040-305-0222"
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}