{
  "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
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Wayne",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82090",
      "recalling_firm": "Maquet Cardiovascular, LLC",
      "address_1": "45 Barbour Pond Dr",
      "address_2": "N/A",
      "postal_code": "07470-2094",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution: US (Nationwide) and countries of: Australia, Belgium, Canada, Czech Republic, France, Germany, Korea, Netherlands, Russia, Spain, Switzerland, and United Kingdom.",
      "recall_number": "Z-0983-2019",
      "product_description": "AXIUS Blower Mister  Product Code/REF Number: CB-1000    The Axius Blower Mister is intended to clear an anastomotic site for improved visibility",
      "product_quantity": "7,880 each (1,576 packs of 5)",
      "reason_for_recall": "Potential lack of carbon dioxide (CO2) flow that may result in a procedural delay during off-pump coronary artery bypass (OPCAB).",
      "recall_initiation_date": "20190124",
      "center_classification_date": "20190307",
      "termination_date": "20200713",
      "report_date": "20190313",
      "code_info": "Lot Numbers: 96255605,96255607,96255608,96255609,96255611  UDI: 20607567700745"
    }
  ]
}