{
  "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": [
    {
      "country": "United States",
      "city": "Wayne",
      "address_1": "550 E Swedesford Rd Ste 400",
      "reason_for_recall": "Customer complaints reporting that the cobb connector detached from the main connector prior to use.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Product Code 115901-000065  Batch Number 13FT06, 13IT05, 13JT08, 13KT12, 14CT11, 14DT03, 14DT24, 14ET04, 14FT04, 14FT20, 14GT10; Product Code 115901-000080 -  Batch Number 13GT16, 13KT18, 13LT08, 14CT11, 14DT03, 14DT24, 14GT15, 14HT12, 14HT20, 14JT04, 14JT12, 14JT21",
      "center_classification_date": "20150819",
      "distribution_pattern": "AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago",
      "state": "PA",
      "product_description": "Bronchial One Lumen Tube - Right",
      "report_date": "20150826",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Teleflex, Inc.",
      "recall_number": "Z-2410-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71727",
      "termination_date": "20170815",
      "more_code_info": "",
      "recall_initiation_date": "20141121",
      "postal_code": "19087-1601",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}