{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Santa Maria",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92867",
      "recalling_firm": "Preat Corp",
      "address_1": "2625 Skyway Dr Ste B",
      "address_2": "N/A",
      "postal_code": "93455-1405",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: FL, CA, OR, TX, OH, CA, SC, OR, NJ, SC,  OUS: None",
      "recall_number": "Z-0153-2024",
      "product_description": "Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental",
      "product_quantity": "23 units",
      "reason_for_recall": "The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage",
      "recall_initiation_date": "20230718",
      "center_classification_date": "20231023",
      "report_date": "20231101",
      "code_info": "UDI-DI: 00842092161388/Lot #OF018357"
    }
  ]
}