{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "country": "United States",
      "city": "Morrisville",
      "address_1": "3015 Carrington Mill Blvd",
      "reason_for_recall": "The tracheal and brochial swivel connectors are incorrectly labeled.",
      "address_2": "",
      "product_quantity": "53 units",
      "code_info": "Catalog: 5-16135; Manufacturing Lot: 73G1600257",
      "center_classification_date": "20191218",
      "distribution_pattern": "US Nationwide distribution in the states of CT, OK, LA, IL, GA, NY, CA, MT, MI, MA, FL.",
      "state": "NC",
      "product_description": "HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 - Product Usage: The Sheridan Endobronchial Tubes are intended for use in Thoracic surgery, brochospirometry, adminitration of endobronchial anesthesia and other uses commonly requiring endobronchial intubation. The Sheridan Endobronchial tube is indicated for main stem bronchus intubation and allows for selective inflation or deflation of either lung.",
      "report_date": "20191225",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Teleflex Medical",
      "recall_number": "Z-0703-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84298",
      "termination_date": "20210930",
      "more_code_info": "",
      "recall_initiation_date": "20191030",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}