{
  "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": "2026-04-22",
    "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": "79396",
      "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": "Worldwide Distribution -- US, Europe, Canada, Australia, and Japan.",
      "recall_number": "Z-1167-2018",
      "product_description": "SwishTapered Implant    Intended for use in support for fixed bridgework.",
      "product_quantity": "1,117 units total",
      "reason_for_recall": "The extender that is packaged with the SwishTapered\" and SwishPlus\" Implant may have been packaged in the incorrect position (upside down in the plastic retainer).",
      "recall_initiation_date": "20180119",
      "center_classification_date": "20180322",
      "termination_date": "20230726",
      "report_date": "20180328",
      "code_info": "Part No. (Lot No.): 934106 (68075, 69252, 79574), 934112 (69101, 80912), 934806 (68076, 75219), 934812 (68078, 68889), 934814 (67980), and 935712 (68077)."
    }
  ]
}