{
  "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": "83086",
      "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 AL, AZ, CA, CO, CT, FL, GA, ID, IL KY, MA, MD, NM, NV, NY, PA, and TX.  There was no government/military distribution.  Foreign distribution was made to Germany, Great Britain, Italy, Spain, Trinidad & Tobago, and UAE.",
      "recall_number": "Z-0010-2020",
      "product_description": "ImplantDirect simply RePlant Implant, size 4.3mmD x 13mmL, 4.3mmD Platform, REF 604313U, Rx, Sterile.  The firm name on the label is Implant Direct Sybron Manufacturing LLC, Thousand Oaks, CA.",
      "product_quantity": "158 devices",
      "reason_for_recall": "The incorrect device was packaged in the vial.",
      "recall_initiation_date": "20180807",
      "center_classification_date": "20191001",
      "report_date": "20191009",
      "code_info": "Lot 108191, UDI (01)10841307108313(17)230118(10)108191"
    }
  ]
}