{
  "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": "2026-04-22",
    "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": "78635",
      "recalling_firm": "Zimmer Dental Inc",
      "address_1": "1900 Aston Ave",
      "address_2": "",
      "postal_code": "92008-7308",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US, Canada, France, Italy, Spain, Germany",
      "recall_number": "Z-0284-2018",
      "product_description": "Tapered Screw-Vent MTX Model TSVTB11",
      "product_quantity": "500 units",
      "reason_for_recall": "Some implant vial caps in the recalled implant lot may inadvertently crack as the result of a manufacturing assembly condition.",
      "recall_initiation_date": "20171120",
      "center_classification_date": "20171221",
      "termination_date": "20240228",
      "report_date": "20171227",
      "code_info": "lot,#63519794; UDI: (01)00889024019935 (17)211130 (10)63519794",
      "more_code_info": ""
    }
  ]
}