{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Westlake Village",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83763",
      "recalling_firm": "Implant Direct Sybron Manufacturing, LLC",
      "address_1": "3050 E Hillcrest Dr",
      "address_2": "N/A",
      "postal_code": "91362-3171",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: IN, VA, MD, TX, WA  OUS: Japan",
      "recall_number": "Z-0364-2020",
      "product_description": "Implant Direct, REF: 833708, Legacy 2 Implant, Surface: HA, 3.7mmD x 8mmL, 3.5mmD Platform, RxOnly, Sterile R, Made in USA    Dental Implants",
      "product_quantity": "23 implants",
      "reason_for_recall": "A QA inspection confirmed that a Healing Collar (Part number 8735-15) was packaged instead of the Implant ordered.",
      "recall_initiation_date": "20190809",
      "center_classification_date": "20191112",
      "termination_date": "20210427",
      "report_date": "20191120",
      "code_info": "Lot #135128  Exp: 3/12/20"
    }
  ]
}