{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Oxford",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71958",
      "recalling_firm": "Villa Radiology Systems LLC",
      "address_1": "91 Willenbrock Rd Ste B1",
      "address_2": "N/A",
      "postal_code": "06478-1036",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution",
      "recall_number": "Z-0129-2016",
      "product_description": "Owandy Radiology I -MAX Touch 3D X-ray",
      "product_quantity": "I-MAX Touch  3D- 6 installed",
      "reason_for_recall": "It has been discovered that due to lack of information accompanying documents the product fails to comply with 21CfR 1020.33(c),1020.33(d),1020.33(g),and 1020.330).",
      "recall_initiation_date": "20150805",
      "center_classification_date": "20151106",
      "termination_date": "20170322",
      "report_date": "20151118",
      "code_info": "p/n 9306251191 and 9306651191"
    }
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}