{
  "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": "2026-04-15",
    "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": "79885",
      "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": "Distribution was made to FL, GA, MD, MI, NC, NY, OR, TX, UT and VA.  There was no foreign/military/government distribution.",
      "recall_number": "Z-1920-2018",
      "product_description": "ImplantDirect Legacy 4 Implant, 5.7mmD x 5.7mmD Platform, Part 885708, Rx, Sterile.  The incorrect cap label shows part 855708, 5.7mmD Platform, 8mmL.",
      "product_quantity": "18 units",
      "reason_for_recall": "The vial cap was mislabeled with the incorrect part number of 855708 but the product description on the cap was correct.  The main vial label was correctly labeled.",
      "recall_initiation_date": "20161115",
      "center_classification_date": "20180523",
      "termination_date": "20180604",
      "report_date": "20180530",
      "code_info": "Lot #71729"
    }
  ]
}