{
  "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": "Orange",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66276",
      "recalling_firm": "Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical",
      "address_1": "1717 W Collins Ave",
      "address_2": "N/A",
      "postal_code": "92867-5422",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution, including Nationwide in the US and the countries of Canada, Great Britain, Australia, France, Germany, Italy, Denmark, Hong Kong, China, Brazil and Saudi Arabia.",
      "recall_number": "Z-2259-2013",
      "product_description": "NX3 Try-In Gel. The product is used as a tooth shade resin material.",
      "product_quantity": "197 units",
      "reason_for_recall": "Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because some of the NX3 Try-In Gel syringes in the affected lot contain a different product material. The material in the affected syringe does not match the shade of the cement as it is labeled.",
      "recall_initiation_date": "20130913",
      "center_classification_date": "20130919",
      "termination_date": "20140211",
      "report_date": "20130925",
      "code_info": "Part Number 33660.  Syringe Lot Number 4580333.  Autobag Lot Number 4584609.",
      "more_code_info": ""
    }
  ]
}