{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Thousand Oaks",
      "address_1": "3050 E Hillcrest Dr",
      "reason_for_recall": "Cap may be mislabeled with incorrect part number, although the correct part number is on the main vial label.",
      "address_2": "",
      "product_quantity": "217 units",
      "code_info": "Part number 8735-05, Lot number 90212",
      "center_classification_date": "20181009",
      "distribution_pattern": "Worldwide distribution.  US nationwide, Canada, Germany, Great Britain, Kuwait, Lithuania, Monaco, Netherlands, and Slovakia.",
      "state": "CA",
      "product_description": "Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile, 3.5mmD Platform.    Dental implant component, used temporarily during impressions for the prosthetic procedure.",
      "report_date": "20181017",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Implant Direct Sybron Manufacturing, LLC",
      "recall_number": "Z-0089-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80297",
      "termination_date": "20200729",
      "more_code_info": "",
      "recall_initiation_date": "20180529",
      "postal_code": "91362",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}