{
  "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": [
    {
      "country": "United States",
      "city": "Santa Ana",
      "address_1": "1851 E Deere Ave",
      "reason_for_recall": "Demonstration Simulus Reusable Sizer Accessory Kits were being incorrectly sourced to customers.  The demonstration product (product used within a wet lab) could have come in contact with non-human (porcine) tissue.",
      "address_2": "",
      "product_quantity": "6",
      "code_info": "GTIN: 00643169707535",
      "center_classification_date": "20200306",
      "distribution_pattern": "US Nationwide distribution in the states of Ohio and Kansas.",
      "state": "CA",
      "product_description": "Medtronic Simulus 750 Flexible Ring/Band Accessory Kit - Product Usage: Used to size a patient's mitral or tricuspid valve in cardiac procedures.",
      "report_date": "20200318",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic CoreValve LLC",
      "recall_number": "Z-1449-2020",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "84837",
      "more_code_info": "",
      "recall_initiation_date": "20200114",
      "postal_code": "92705-5720",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}