{
  "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-0996-2014",
      "product_description": "Medtronic Select 3D Arterial Cannulae.  Vented, model 78622  (22 Fr.).  Non-Vented Cannulae, model 78722 (22 Fr.).  Sterilized using Ethylene Oxide.  Non-pyrogenic.      The Cannula consists of a curved, angled or beveled tip with or without flange that is permanently attached to a molded, clear, flexible PVC tapered body or wirebound PVC body.  The cannula body features a tip orientation line to indicate direction of the cannula tip during cannulation.  The proximal end of the cannula includes a connection site or a molded 0.95 cm (3/8 in) barbed connector with or without a molded plastic vent plug or peel cap.  The vent plug or peel cap allows air to be vented from the cannula before connection to the perfusion line.     These cannulae are intended for use in perfusion of the ascending aorta during short term (6 hours or less) cardiopulmonary bypass.",
      "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 78622, Lot numbers:  2011031714, 2011040345, 2011050373, 2011060471,   2011060641, 2011060642, 2011070099, 2011072408, 2011081502, 2011102965,   2011111215, 2011120575, 2012011143, 2012011425, 2012020052, 2012040536,   2012051387, 2012090216, 2012101333 ,2013010957, 2013011791, 2013020303,   2013030729, 2013040209, 2013040282, 2013040710, 2013041272, 2013051447,   2013060736, 2013071836, 2013072009, 201105C105, 201203C854.      Model 78722, Lot numbers:  2011031588, 2011031885, 2011051006, 2011051226,   2011061585, 2011071672, 2011082216, 2011091825 , 2011101670, 2011102093,   2011110717, 2011120059, 2012060478, 2012061056, 2012061057, 2012061725,   2012070570, 2012090657, 2013011121, 2013021260, 2013030685, 2013040494,   2013040595, 2013070162, 2013070483, 2013081289, 2013081603, 201108C227.",
      "more_code_info": ""
    }
  ]
}