{
  "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": [
    {
      "status": "Terminated",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83038",
      "recalling_firm": "Medtronic Inc",
      "address_1": "710 Medtronic Pkwy Mailstop Ls245",
      "address_2": "N/A",
      "postal_code": "55432-5603",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of TN, NY, NJ, and countries of France, Italy, Libya, Poland, Spain.",
      "recall_number": "Z-1882-2019",
      "product_description": "Hancock II T510 Bioprosthesis, Mitral, REF T505U227 -  Product Usage: Replacement of malfunctioning native or prosthetic aortic and/or mitral valves.",
      "product_quantity": "5 units",
      "reason_for_recall": "Fifteen affected devices were distributed worldwide, which were mislabeled with an incorrect size. In all cases, the actual surgical heart valves are larger than what was indicated on the boxes and jar labels.",
      "recall_initiation_date": "20190521",
      "center_classification_date": "20190626",
      "termination_date": "20201007",
      "report_date": "20190703",
      "code_info": "GTIN: 00643169000261  Serial Numbers:  B167637, B192698, B217347, B217329, B217330"
    }
  ]
}