{
  "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": "76208",
      "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 : PA, MA, CO, OH, NJ, GA, CA, TX, IL, VA, MN, NH, WA, SC, AZ, LA, MD, OK, IN, NY, NC and KS.",
      "recall_number": "Z-1036-2017",
      "product_description": "Olympus Scientific Solutions Americas Corporation  (\u001cOSSA\u001d) VANTA¿ XRF Analyzer. Model Vanta VCR and Vanta VMR   Analytical X-ray systems",
      "product_quantity": "US 74",
      "reason_for_recall": "It was discovered under rare circumstances the LED warning light circuit could fail. If this happens, while the instrument is emitting X-rays during at test, the LED warning lights will not illuminate. The test runs normally and will execute as before, but the light will not be on.",
      "recall_initiation_date": "20170107",
      "center_classification_date": "20170201",
      "termination_date": "20190827",
      "report_date": "20170208",
      "code_info": "affects all units.",
      "more_code_info": ""
    }
  ]
}