{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Waltham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75575",
      "recalling_firm": "Olympus Scientific Solutions Americas",
      "address_1": "48 Woerd Ave",
      "address_2": "N/A",
      "postal_code": "02453-3824",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : TX, WA, GA, MA, SC, AZ, PA, VA, CA, OH, NJ, MD, CO, IL, LA, and MN.",
      "recall_number": "Z-0680-2017",
      "product_description": "Olympus Scientific Solutions Americas Corporation (\u001cOSSA\u001d) Model: VANTA Analytical X-Ray System",
      "product_quantity": "41 units",
      "reason_for_recall": "Possible unintentional x-ray emission after users attempt early termination of the sequence.",
      "recall_initiation_date": "20161027",
      "center_classification_date": "20161207",
      "termination_date": "20200730",
      "report_date": "20161214",
      "code_info": "Model - Vanta VCR"
    }
  ]
}