{
  "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": "Santa Ana",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69089",
      "recalling_firm": "Medtronic Cardiovascular Surgery-the Heart Valve Division",
      "address_1": "1851 E Deere Ave",
      "address_2": "N/A",
      "postal_code": "92705-5720",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of MD and TX.",
      "recall_number": "Z-2623-2014",
      "product_description": "Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No. 0174ACP012.    Used use in conjunction with Hancock Conduit Model 105  to provide an alternate method for relief of left ventricular hypertension.",
      "product_quantity": "2 units",
      "reason_for_recall": "Medtronic has decided to discontinue production and distribution of this low-volume product.",
      "recall_initiation_date": "20140815",
      "center_classification_date": "20140911",
      "termination_date": "20141106",
      "report_date": "20140917",
      "code_info": "Serial Numbers: B146341, B146350"
    }
  ]
}