{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Federal Way",
      "state": "WA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98823",
      "recalling_firm": "Sagemax Bioceramics, Inc.",
      "address_1": "34210 9th Ave S Ste 118",
      "address_2": "N/A",
      "postal_code": "98003-6790",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of CA, MO, MN, NY, FL, ID and the countries of AT, CZ, DE, EE, EG, FR, GR, ID, IT, KZ, RS, SE, SI, TZ, VN.",
      "recall_number": "Z-2356-2026",
      "product_description": "NexxZr T Multi A3.5 W98-16mm, REF: 745451",
      "product_quantity": "113",
      "reason_for_recall": "Yttrium-stabilized zirconium oxide discs for fixed all-ceramic dental restorations may have  reduced or missing dentin layer and when used clinically in the patient's mouth there is an increased risk of fractures under functional stress.",
      "recall_initiation_date": "20251211",
      "center_classification_date": "20260609",
      "report_date": "20260617",
      "code_info": "UDI-DI: 00842271175373, Lot: YBDGLD"
    }
  ]
}