{
  "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": "Romulus",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68426",
      "recalling_firm": "Kerr Corporation",
      "address_1": "28200 Wick Rd",
      "address_2": "N/A",
      "postal_code": "48174-2639",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of Canada, Mexico, Australia, Belgium, Czech Republic, Germany, Spain, France, Great Britain, French Guiana, Italy, Portugal, and Saudi Arabia.",
      "recall_number": "Z-1788-2014",
      "product_description": "Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294.    The intended use of this device is to be used as a dental restorative material in the treatment of dental caries.",
      "product_quantity": "2,030 units",
      "reason_for_recall": "Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number 29948, Lot Number 3-1294), because it may set faster than specified in the Directions for Use.",
      "recall_initiation_date": "20140529",
      "center_classification_date": "20140613",
      "termination_date": "20141027",
      "report_date": "20140625",
      "code_info": "Part Number 29948, Lot Number 3-1294.  Expires October 2016",
      "more_code_info": ""
    }
  ]
}