{
  "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": "Elkton",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81094",
      "recalling_firm": "Terumo Cardiovascular Systems Corporation",
      "address_1": "125 Blue Ball Rd",
      "address_2": "N/A",
      "postal_code": "21921-5315",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide in the states of FL, IL, NY, OH, TX.    The products were distributed to the following foreign country:  Singapore.",
      "recall_number": "Z-0227-2019",
      "product_description": "VirtuoSaph Plus Endoscopic Vessel Harvesting System, Catalog Number: VSP550EX    Product Usage:  The VittuoSaph¿ Plus Endoscopic Vessel Harvesting System VSP550EX is indicated for use in minimally invasive surgery allowing access for vessel harvesting, and is primarily indicated for patients undergoing endoscopic surge1y for arterial bypass. It is indicated for cutting tissue and controlling bleeding through coagulation, and for patients requit¿ing blunt dissection of tissue including dissection of blood vessels and dissection of blood vessels of the extremities. Extremity procedures include tissue dissection and/or vessel harvesting along the saphenous vein for coronary artery bypass grafting and peripheral artery bypass grafting or radial artery for use in coronary artery bypass grafting   vc",
      "product_quantity": "135",
      "reason_for_recall": "The system's IFU contains a list of generators that the have been deemed compatible.  Recent reports indicate that one energy platform is not compatible with the system.  Therefore, it has been removed from the list of compatible generators within the IFU.",
      "recall_initiation_date": "20180831",
      "center_classification_date": "20181023",
      "termination_date": "20191021",
      "report_date": "20181031",
      "code_info": "Lot Numbers: 81K"
    }
  ]
}