{
  "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": "Ongoing",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89754",
      "recalling_firm": "Medtronic Inc",
      "address_1": "710 Medtronic Pkwy Mailstop Ls245",
      "address_2": "",
      "postal_code": "55432-5603",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide and the countries of Canada.",
      "recall_number": "Z-0927-2022",
      "product_description": "Harmony Delivery Catheter System.  Part of the Harmony Transcatheter Pulmonary Valve (TPV) Replacement Implantation System.",
      "product_quantity": "1483 devices",
      "reason_for_recall": "There is potential for the capsule bond to break during the procedure.",
      "recall_initiation_date": "20220302",
      "center_classification_date": "20220418",
      "report_date": "20220427",
      "code_info": "HARMONY-DCS (GTIN: 00763000341367);  Lot Numbers: 0010519040, 0010565921, 0010578123, 0010578126, 0010583884, 0010631963, 0010631969, 0010631971, 0010717000, 0010717001, 0010717002, 0010723188, 0010723189, 0010723190, 0010727345, 0010804938, 0010826589, (the following lots were added 4/22/2022) 0010826591, 0010826592, and 0010826593",
      "more_code_info": ""
    }
  ]
}