{
  "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": "83794",
      "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": "US distribution in the states of:  CA, UT, VA, NY, IL, AR, TX, OH, NV, FL, ID, AK, NC, KS, MN, AZ, CO,",
      "recall_number": "Z-0363-2020",
      "product_description": "Implant Direct, REF654311U, simply InterActive Implant, Surface: SBM, Qty 1, 4.3mmD x 11.5mmL, 3.4mmD Platform, RX only, Sterile R    Dental Implant",
      "product_quantity": "53 implants",
      "reason_for_recall": "packaging error;  An internal  QA inspection revealed that a incorrect healing collar could have been packaged in  an implant assembly kit.",
      "recall_initiation_date": "20181026",
      "center_classification_date": "20191112",
      "report_date": "20191120",
      "code_info": "Lot numbers 120197; Exp. 07/16/2023 and 120198; Exp. 07/19/2023"
    }
  ]
}