{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Mettawa",
      "address_1": "26125 N Riverwoods Blvd",
      "reason_for_recall": "Vyaire Medical has discovered potential patient safety risk with associated with the Tri-Flow Subglottic Suction System. The distal soft tip of the catheter has been identified as having the potential to break off during patient use and result in aspiration of a solid foreign body.",
      "address_2": "",
      "product_quantity": "2150 Units Total",
      "code_info": "Part number: CM28010;    Lot/Serial Numbers:  0001158835 , 0001158836, 0001158837, 0001185564,  0001194114 , 0004008255, 0004008256.",
      "center_classification_date": "20180821",
      "distribution_pattern": "Domestic Distribution:  AZ, CA, CT, FL, GA, IA, IL, IN, MA, MD, MN,  NJ, OH, OK, SD, TX, WA, WI.",
      "state": "IL",
      "product_description": "The Tri-Flo Subglottic Suction System",
      "report_date": "20180829",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Vyaire Medical",
      "recall_number": "Z-2826-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80508",
      "termination_date": "20200728",
      "more_code_info": "",
      "recall_initiation_date": "20180620",
      "postal_code": "60045-3420",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}