{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Minnetonka",
      "address_1": "16200 State Highway 7",
      "reason_for_recall": "Leak issues were discovered through accelerated age testing.",
      "address_2": "Unit B",
      "product_quantity": "2",
      "code_info": "Lot numbers: 101637, 101640",
      "center_classification_date": "20140515",
      "distribution_pattern": "Distribution to TN only",
      "state": "MN",
      "product_description": "InterValve V8 Balloon Aortic Valvuloplasty Catheter, model  172212C110, 192412C110, 212612C110, 232812C110.  Used in Cardiovascular procedures for Balloon Aortic Valvuloplasty.",
      "report_date": "20140521",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "InterValve Inc",
      "recall_number": "Z-1621-2014",
      "initial_firm_notification": "Visit",
      "product_type": "Devices",
      "event_id": "67964",
      "termination_date": "20140616",
      "more_code_info": "",
      "recall_initiation_date": "20140314",
      "postal_code": "55345",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}