{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Santa Maria",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91876",
      "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 Nationwide distribution in the states of TX, OR, UT, NY.",
      "recall_number": "Z-1285-2023",
      "product_description": "Neodent GM X 6mm Engaging Titanium Base, REF: 9007162",
      "product_quantity": "26",
      "reason_for_recall": "Engaging titanium base contains a dimensional condition that allows vertical movement of the titanium base after the prosthetic screw is torqued to the recommended value, which if undetected and installed on the implant, may lead to abutment/screw fracture, which could result in the abutment/screw/crown being ingested by the patient.",
      "recall_initiation_date": "20230221",
      "center_classification_date": "20230324",
      "report_date": "20230405",
      "code_info": "UDI: 00842092161326, Lots: 211891 and 211912"
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}