{
  "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": "84377",
      "recalling_firm": "Maquet Cardiovascular Us Sales, 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": "The products were distributed to the following US states:  ME, NV, NY, OH, PA, TX, and VA.",
      "recall_number": "Z-0678-2020",
      "product_description": "Maquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive, Model Number 701022161.  The device is a component of the ROTAFLOW System Console.",
      "product_quantity": "11 distributed in the US",
      "reason_for_recall": "A loose ODU plug / Coaxial cable connection may result in fluctuating flow values on the Console.",
      "recall_initiation_date": "20191203",
      "center_classification_date": "20191212",
      "termination_date": "20200918",
      "report_date": "20191218",
      "code_info": "UDI: 04037691258997;  Serial Numbers 9348936  910114412  910114420  910114429  910114430  910114432  910114435  910114438  910117243  91064722  91067680",
      "more_code_info": ""
    }
  ]
}