{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Bethel Park",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72396",
      "recalling_firm": "Instrumentation Industries Inc",
      "address_1": "2990 Industrial Blvd",
      "address_2": "N/A",
      "postal_code": "15102-2536",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US including PA, FL, GA, WA, OH, CA, KA and Internationally to Canada.",
      "recall_number": "Z-0269-2016",
      "product_description": "Ventilator Tubing",
      "product_quantity": "567",
      "reason_for_recall": "As a distributor of tubing manufactured by Smooth Bore Plastics, we are initiating a product recall for specific lots of KC 036, KC 060 and KC 072 reusable ventilator tubes due to a possible manufacturing defect:  A few tubes may have the potential for delamination to occur between the layers of the tube wall which, should it occur, would result in leakage",
      "recall_initiation_date": "20150923",
      "center_classification_date": "20151112",
      "termination_date": "20161128",
      "report_date": "20151118",
      "code_info": "Model Length Lot Numbers  KC 036 36\u001d tube P0614015, P0818215, P0825515    KC 060 60\u001d tube P0511915, P0608315  KC 072 72\u001d tube P0618415, P0818515"
    }
  ]
}