{
  "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": "2026-07-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Ventura",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98509",
      "recalling_firm": "TMJ Solutions Inc",
      "address_1": "6059 King Dr",
      "address_2": "N/A",
      "postal_code": "93003-7607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the state of MA.",
      "recall_number": "Z-2524-2026",
      "product_description": "TMJ Bilateral Implants, REF: CHG020",
      "product_quantity": "1",
      "reason_for_recall": "Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.",
      "recall_initiation_date": "20260211",
      "center_classification_date": "20260622",
      "report_date": "20260701",
      "code_info": "UDI-DI: 07613327626575, Lot: 2508181038"
    }
  ]
}