{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85092",
      "recalling_firm": "MEDTRONIC ATS MEDICAL, INC.",
      "address_1": "3800 Annapolis Ln N",
      "address_2": "N/A",
      "postal_code": "55447-5439",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "China",
      "recall_number": "Z-1533-2020",
      "product_description": "Medtronic Open Pivot Aortic Valve Graft, REF 502AG25, SIZE 25 mm",
      "product_quantity": "2 devices",
      "reason_for_recall": "Medtronic received a complaint from China that the label on the box for an Open Pivot Heart Valve was labeled as Aortic, but the product was Mitral.  The valve itself was correctly labeled as Mitral.",
      "recall_initiation_date": "20200211",
      "center_classification_date": "20200320",
      "termination_date": "20220304",
      "report_date": "20200401",
      "code_info": "UDI 00643169297913, Serial Numbers:  935603, 935732",
      "more_code_info": ""
    }
  ]
}