{
  "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": "Durham",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68493",
      "recalling_firm": "Teleflex Medical",
      "address_1": "4024 Stirrup Creek Dr",
      "address_2": "",
      "postal_code": "27703-9000",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of Belgium, Canada, China, Germany, Great Britain, France, India, Malaysia, Mexico, Philippines, Singapore, Thailand and Zambia.",
      "recall_number": "Z-2005-2014",
      "product_description": "Aquapak 101 SW, 190, mL w/040 Adaptor, Japan, Teleflex Medical, respiratory gas humidifier adaptor",
      "product_quantity": "7,758,650 ea. (total for all types listed)",
      "reason_for_recall": "The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.",
      "recall_initiation_date": "20140605",
      "center_classification_date": "20140707",
      "termination_date": "20150702",
      "report_date": "20140716",
      "code_info": "Product Code: 001-40J, Lot numbers: 001129 & 002129.",
      "more_code_info": ""
    }
  ]
}