{
  "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": [
    {
      "country": "United States",
      "city": "Wayne",
      "address_1": "45 Barbour Pond Drive",
      "reason_for_recall": "A technical alarm may be generated on the FLOW-i system when using the MAN/AUTO switch to change ventilation modes from manual to automatic or from automatic to manual if the switch is not fully engaged in the \"on\" or \"off\" position but remains in the \"in-between\u001d position.",
      "address_2": "",
      "product_quantity": "284 units",
      "code_info": "Model Number :6677300  Serial Number : 1170",
      "center_classification_date": "20120706",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) state of GA only and countries of:  Argentina, Australia, Austria, Belgium, China, Czech Republic, Ecuador, Finland, France, Germany, India, Ireland, Israel, Italy, Latvia, Netherlands, Norway, Poland, Portugal, Romania, Russia, Serbia, Singapore, South Africa, Spain, Sweden incl Maquet Critical Care, Switzerland, Thailand, United Arab Emirates, and United Kingdom.",
      "state": "NJ",
      "product_description": "FLOW-I Anesthesia System    The system is intended for use in administrating anesthesia while controlling the entire ventilation for patients with no ability to breathe, as well as in supporting patients with a limited ability to breathe.",
      "report_date": "20120718",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Maquet Cardiovascular Us Sales, Llc",
      "recall_number": "Z-1925-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62118",
      "termination_date": "20150909",
      "more_code_info": "",
      "recall_initiation_date": "20120220",
      "postal_code": "07470",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}