{
  "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": "Terminated",
      "city": "Carrollton",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89569",
      "recalling_firm": "Brius Technologies Inc.",
      "address_1": "2611 Westgrove Dr",
      "address_2": "",
      "postal_code": "75006-2349",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide:  CA, DC, MA, NJ, NY, TX",
      "recall_number": "Z-0888-2022",
      "product_description": "Brius Pontics (components in a set of custom metal orthodontic devices);BRIUS , RX Only, Non-Sterile, Custom Made Device, ID:  52345400UL",
      "product_quantity": "6",
      "reason_for_recall": "Pontics, brackets, and customized orthodontic appliances were sold and distributed prior to completing the standard design control process, being documented, and released.",
      "recall_initiation_date": "20220207",
      "center_classification_date": "20220407",
      "termination_date": "20241018",
      "report_date": "20220413",
      "code_info": "524947 .00BB (upper); 524925 .00BB (upper); 524503 .10Bn (upper); 523431 .20U; 524304 .10Bn (upper); 523595 .21bn (upper)",
      "more_code_info": ""
    }
  ]
}