{
  "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": "77759",
      "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": "Worldwide Distribution - USA (nationwide) Distribution",
      "recall_number": "Z-2760-2017",
      "product_description": "Olympus Scientific Solutions Americas Corporation (\u001cOSSA\u001d) Model: VANTA Analytical X-Ray System, X-Ray Fluorescence",
      "product_quantity": "146 units",
      "reason_for_recall": "Instruments may, under certain specific circumstances listed below, fail to stop when a test is initiated and no sample is present (proximity shut down fails to end test).",
      "recall_initiation_date": "20170711",
      "center_classification_date": "20170802",
      "termination_date": "20230503",
      "report_date": "20170809",
      "code_info": "Models : VCR and VMR."
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}