{
  "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": [
    {
      "country": "United States",
      "city": "Thousand Oaks",
      "address_1": "3050 E Hillcrest Dr",
      "reason_for_recall": "Due to out of specification, the clinician would not be able to fit and engage the abutment with the implant",
      "address_2": "",
      "product_quantity": "60 units",
      "code_info": "Lot numbers: 45353, 66011, and 75850",
      "center_classification_date": "20180705",
      "distribution_pattern": "CA, FL, GA, IL, LA, MI, MT, NC, NJ, NY, OK, OR, SC, SD, TN & WA; International: Jordan, Great Britain, Germany, Spain, Italy & Poland",
      "state": "CA",
      "product_description": "REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60",
      "report_date": "20180711",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Implant Direct Sybron Manufacturing, LLC",
      "recall_number": "Z-2376-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80281",
      "termination_date": "20200713",
      "more_code_info": "",
      "recall_initiation_date": "20180518",
      "postal_code": "91362",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}