{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Glendora",
      "address_1": "1332 S Lone Hill Ave",
      "reason_for_recall": "SybronEndo is recalling the Sealapex Xpress because it was labeled with an incorrect expiration date of 2017-11 while the syringe was labeled with the correct expiration date of 2016-11.",
      "address_2": "",
      "product_quantity": "179 units",
      "code_info": "lot # 5-1310",
      "center_classification_date": "20160916",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and countries of: Canada, Australia, Mexico, Belgium, Denmark, Germany, Great Britain, and Sweden.",
      "state": "CA",
      "product_description": "Sealapex Xpress, Part No. 33639    The brand name of the device is Sealapex Xpress, a root canal filling resin. Sealapex Xpress is intended to be used during endodontic therapy to fill the root canal of a tooth.",
      "report_date": "20160928",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ormco/Sybronendo",
      "recall_number": "Z-2836-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75114",
      "termination_date": "20170901",
      "more_code_info": "",
      "recall_initiation_date": "20160831",
      "postal_code": "91740-5339",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}