{
  "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": "2026-03-18",
    "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": "91067",
      "recalling_firm": "X-NAV Technologies, LLC",
      "address_1": "1555 Bustard Rd Ste 75",
      "address_2": "N/A",
      "postal_code": "19446-5731",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution and Foreign country of: Canada",
      "recall_number": "Z-0222-2023",
      "product_description": "X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or performing XMark registration.  Catalog Number:P010673",
      "product_quantity": "102 units",
      "reason_for_recall": "Product missing one of two welds connecting the tip to the shaft, if the remaining weld breaks, it is possible that the tip could fall out during X-Mark registration and fall into the patient s mouth. In this case, the patient may aspirate or swallow the probe tip.",
      "recall_initiation_date": "20220928",
      "center_classification_date": "20221110",
      "report_date": "20221116",
      "code_info": "UDI-DI: (01)00817421020995 (10) 2007010010  Lot number: 2007010010"
    }
  ]
}