{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Carlsbad",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69392",
      "recalling_firm": "Zimmer Dental Inc",
      "address_1": "1900 Aston Ave",
      "address_2": "N/A",
      "postal_code": "92008-7308",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-US (nationwide) and the countries of  Poland, Canada, Belgium, Italy, France, Israel, Morocco, Spain, Costa Rica, and Japan.",
      "recall_number": "Z-0153-2015",
      "product_description": "Spline Twist Implant, HA 3.25mmD X 15mmL; Part No. 2135.    Zimmer Dental Spline implant systems are designed for use in edentulous mandibles or maxillae for attachment of complete denture prostheses for immediate or conventional loading, or as a terminal or intermediary abutment for fixed or removable bridgework, or as a free standing single tooth replacement.",
      "product_quantity": "1,044 units",
      "reason_for_recall": "Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect diameter size was printed on the inner vial.",
      "recall_initiation_date": "20141001",
      "center_classification_date": "20141030",
      "termination_date": "20150428",
      "report_date": "20141105",
      "code_info": "Lot No. 61792330",
      "more_code_info": ""
    }
  ]
}