{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lansdale",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94175",
      "recalling_firm": "X-NAV Technologies, LLC",
      "address_1": "1555 Bustard Rd Ste 75",
      "address_2": "",
      "postal_code": "19446-5731",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of China, Europe, Japan.",
      "recall_number": "Z-1393-2024",
      "product_description": "X-Guide Handpiece Adaptor Sleeve 3, Model P010727",
      "product_quantity": "154 units",
      "reason_for_recall": "The Handpiece Adaptor may have a manufacturing defect causing incorrect geometry. The incorrect geometry in turn causes the Handpiece Adaptor to not fit onto the doctor's dental handpiece.",
      "recall_initiation_date": "20240304",
      "center_classification_date": "20240329",
      "report_date": "20240410",
      "code_info": "UDI-DI: 00817421021503; Lot: 2306020012, 2310010012",
      "more_code_info": ""
    }
  ]
}