{
  "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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  "results": [
    {
      "status": "Ongoing",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92394",
      "recalling_firm": "Covidien, LLC",
      "address_1": "161 Cheshire Ln N Ste 100",
      "address_2": "N/A",
      "postal_code": "55441-5433",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "International distribution in the country of Taiwan.",
      "recall_number": "Z-2008-2023",
      "product_description": "Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS",
      "product_quantity": "1 unit",
      "reason_for_recall": "Single ILLUMISITE Platform Console was converted from a 220-240VAC model to a 120VAC configuration using a non-supplied power cord and non-supplied fuses in the field by Medtronic Field Service Engineer.",
      "recall_initiation_date": "20230522",
      "center_classification_date": "20230626",
      "report_date": "20230705",
      "code_info": "UDI-DI: 10884521782211; Serial Number: 518503",
      "more_code_info": ""
    }
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}