{
  "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": [
    {
      "status": "Terminated",
      "city": "Westlake Village",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84777",
      "recalling_firm": "Implant Direct Sybron Manufacturing LLC",
      "address_1": "3050 E Hillcrest Dr",
      "address_2": "",
      "postal_code": "91362-3171",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: AR, AZ, CA, ID, IL, IN, KY, MD, ND, NH, NJ, NV, NY, Oh, OR, PA, TX, UT, WA, WI, WV, GA,MO",
      "recall_number": "Z-1157-2020",
      "product_description": "Implant Direct, CE 0086, REF: 855710, Legacy 3 Impant, Surface: SBM, Qty:1, Size:5.7mmD x 10mmL, 5.7mmD Platform, RxOnly, Sterile R,",
      "product_quantity": "78 implants",
      "reason_for_recall": "Through a customer complaint and and internal investigation it was determined that some implant packages contain the incorrect cover screw and extender.  This could result in delay in surgery and/or  a potential  new surgical procedures to place the correct parts. The level of severity varies based on a one or two stage surgery.",
      "recall_initiation_date": "20191011",
      "center_classification_date": "20200212",
      "termination_date": "20240412",
      "report_date": "20200219",
      "code_info": "Lot # 68209",
      "more_code_info": ""
    }
  ]
}