{
  "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": {
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      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82451",
      "recalling_firm": "Gyrus ACMI, Inc.",
      "address_1": "2925 Appling Rd",
      "address_2": "N/A",
      "postal_code": "38133-3901",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "product_description": "Olympus Diego Elite Console  MDCONS 100",
      "product_quantity": "US: 107 consoles, OUS: 157 consoles",
      "reason_for_recall": "Olympus Diego Elite Consoles may inadvertently permit activation of the RF energy feature when used with Diego Elite blades",
      "recall_initiation_date": "20190308",
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