{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Kalona",
      "state": "IA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88906",
      "recalling_firm": "Civco Medical Instruments Co. Inc.",
      "address_1": "102 1st St S",
      "address_2": "N/A",
      "postal_code": "52247-9589",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Belgium, Canada, China (Mainland), China (Taiwan), Denmark, France, Germany, Italy, Japan, Netherlands, Singapore, South Korea, Spain, Thailand.",
      "recall_number": "Z-0395-2022",
      "product_description": "VirtuTRAX Instrument Navigator, Sensor with 14 Ga VirtutTRAX",
      "product_quantity": "52 boxes (5 units/box)",
      "reason_for_recall": "There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.",
      "recall_initiation_date": "20211008",
      "center_classification_date": "20211220",
      "termination_date": "20240930",
      "report_date": "20211229",
      "code_info": "Part Number 5350925; UDI 00841436100892; Lot Numbers: A117795, A119539, A121993, A129844, A131074, A131075, A131690, A142178"
    }
  ]
}