{
  "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": [
    {
      "country": "United States",
      "city": "Westlake Village",
      "address_1": "3050 E Hillcrest Dr",
      "reason_for_recall": "Consignees received product 6060-62, Replant Overdenture Abutment with the label for 4500-61 GoDirect Screw-Retaining Top.",
      "address_2": "",
      "product_quantity": "14",
      "code_info": "Lot #75808",
      "center_classification_date": "20170109",
      "distribution_pattern": "U.S. distribution to the following; WA.    Foreign distribution to the following; Netherlands.",
      "state": "CA",
      "product_description": "GoDirect Screw-Retaining Top  Part Numbers: 4500-61",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Implant Direct Sybron Manufacturing, LLC",
      "recall_number": "Z-0961-2017",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "75838",
      "termination_date": "20170216",
      "more_code_info": "",
      "recall_initiation_date": "20161128",
      "postal_code": "91362-3171",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}