{
  "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": "Burlington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82374",
      "recalling_firm": "Keystone Dental Inc",
      "address_1": "154 Middlesex Tpke",
      "address_2": "N/A",
      "postal_code": "01803-4403",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "FL, MA, SC, VA",
      "recall_number": "Z-1062-2019",
      "product_description": "Paltop Fully Guided Surgical Kit- containing the 1.25mm Hex Driver  For surgical and restorative applications prosthetic devices, such as artificial teeth  Part Number: 30-70021",
      "product_quantity": "1 hex Driver",
      "reason_for_recall": "Paltop Surgical Kits contain 1.25mm Hex Driver(s) which may have a slightly oversized hex driving feature, make it difficult to engage screws and abutments containing the corresponding screw feature",
      "recall_initiation_date": "20190222",
      "center_classification_date": "20190327",
      "termination_date": "20200619",
      "report_date": "20190403",
      "code_info": "Lot Numbers: WO-010366"
    }
  ]
}