{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Westlake Village",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84801",
      "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. Nationwide distribution in the states of:  KS, LA, OH, RI, CA, NJ, MA, FL, UT, ID, MO, WY, WI, PA, WA.    O.U.S. (Foreign): DE, IT, HU, JP",
      "recall_number": "Z-1041-2020",
      "product_description": "Legacy 3 Implant, Size: 4.2mmD x 13mmL, 3.5mmD Platform, REF: 864213",
      "product_quantity": "72",
      "reason_for_recall": "Some dental implant packages contain incorrect implants, which could lead to surgery rescheduling.",
      "recall_initiation_date": "20191007",
      "center_classification_date": "20200205",
      "termination_date": "20210428",
      "report_date": "20200212",
      "code_info": "Lot: 83327"
    }
  ]
}