{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Noblesville",
      "address_1": "15011 Herriman Blvd",
      "reason_for_recall": "King Systems received a customer complaint indicating that the customer had ordered a breathing circuit with a Latex breathing bag.  The product they received contained a Latex breathing bag, but was labeled as non-latex.",
      "address_2": "",
      "product_quantity": "1 case; 40 units",
      "code_info": "Part Number DF4110-61  Lot Number I063N",
      "center_classification_date": "20130927",
      "distribution_pattern": "Nationwide Distribution - NE only.",
      "state": "IN",
      "product_description": "Universal Flex2 Breathing Circuit  Class I   510(k) Exempt    An anesthesia breathing circuit is a device that is intended to administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Y-piece.",
      "report_date": "20131009",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "King Systems Corp.",
      "recall_number": "Z-2272-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66184",
      "termination_date": "20131118",
      "more_code_info": "",
      "recall_initiation_date": "20120823",
      "postal_code": "46060-4253",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}