{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Brooklyn Park",
      "address_1": "7611 Northland Dr N",
      "reason_for_recall": "EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.",
      "address_2": "",
      "product_quantity": "221 (111 US, 110 OUS)",
      "code_info": "Lot number 2015060544;",
      "center_classification_date": "20150819",
      "distribution_pattern": "Worldwide distribution. US nationwide including: FL, GA, IL, MI, NY, NC, PA, WV; Germany, Hong Kong, and Italy.",
      "state": "MN",
      "product_description": "Medtronic EOPA Arterial Cannula,  Model # 77620.  Lot: 2015060544 intended to deliver oxygenated blood to the heart during cardiopulmonary bypass procedures for up to 6 hours in duration.",
      "report_date": "20150826",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Perfusion Systems",
      "recall_number": "Z-2420-2015",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "71897",
      "termination_date": "20160404",
      "more_code_info": "",
      "recall_initiation_date": "20150724",
      "postal_code": "55428-1088",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}