{
  "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": "Ongoing",
      "city": "Reno",
      "state": "NV",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77617",
      "recalling_firm": "Hamilton Medical, Inc.",
      "address_1": "4990 Energy Way",
      "address_2": "N/A",
      "postal_code": "89502-4123",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to IL and TX.",
      "recall_number": "Z-0335-2018",
      "product_description": "Intellicuff Standalone (PN 951001)    Used to continuously measure and automatically maintain the user-set cuff pressure of an endotracheal tube or tracheostomy tube during mechanical ventilation. Used in the ventilation of adults, pediatrics, and neonates.",
      "product_quantity": "176 units",
      "reason_for_recall": "Issue related to the performance of the motor in recalled product. During use, motor may cease to function.",
      "recall_initiation_date": "20170620",
      "center_classification_date": "20180112",
      "report_date": "20180124",
      "code_info": "Serial No. 1000 thru 2090; P/N 951001"
    }
  ]
}