{
  "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": [
    {
      "status": "Terminated",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67400",
      "recalling_firm": "Medtronic Inc. Cardiac Rhythm Disease Management",
      "address_1": "8200 Coral Sea St NE",
      "address_2": "",
      "postal_code": "55112-4391",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution: US (Nationwide) including Puerto Rico, and Internationally to: Algeria, Argentina, Austria, Belgium, Bosnia And Herzegovina, Brazil, Canada, Cyprus, El Salvador, France, Georgia, Germany, Greece, Hungary, India, Ireland, Italy, Japan, Jordan, Kuwait, Netherlands, Oman, Paraguay, Poland, Portugal, Russian Federation, Saudi Arabia, Slovakia, Spain, Sweden, Switzerland, Thailand, Turkey, United Kingdom, Venezuela, and Yemen.",
      "recall_number": "Z-1000-2014",
      "product_description": "Medtronic Intersept Custom Tubing Pack which contain Select 3D or Select CAP Arterial Cannulae.  Model 3Y90R3, the following model is only approved in Europe C300901B.  Sterilized using Ethylene Oxide.  Non-pyrogenic.      The design and components of this product are specified by the user.      This product is indicated for use in the extracorporeal circuit during cardiopulmonary bypass procedures.",
      "product_quantity": "19483 total (7669 US, 11814 OUS)",
      "reason_for_recall": "Medtronic is recalling all models of its Select 3D and Select CAP Arterial Cannula product families due to reports of the cannula body splitting near the suture collar.",
      "recall_initiation_date": "20140130",
      "center_classification_date": "20140219",
      "termination_date": "20141006",
      "report_date": "20140226",
      "code_info": "Model 3Y90R3, Lot numbers:  12227513, 12277464, 206420618, 206618641, 206842458, 206932996, 207184816.      Model C300901B, Lot number 206499164.",
      "more_code_info": ""
    }
  ]
}