{
  "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": [
    {
      "country": "United States",
      "city": "Maple Grove",
      "address_1": "6464 Sycamore Ct N",
      "reason_for_recall": "Vascular Solutions, Inc. (VSI) is voluntarily removing all lots of Venture catheters due to a potential problem.  Venture RX (Model 5820), Venture OTW (Model 5821), and Venture CS (Model 5822) catheters. After an internal investigation, VSI determined that material used in catheter construction may detach from within the lumen of the distal tip during use.",
      "address_2": "",
      "product_quantity": "13,551 (7,054 are unexpired)",
      "code_info": "581713 582455 582588 583022 583409 583410 584469 584470 599777  584471 585180 585458 585459 585787 586408 586972 587035  587036 587408 587775 588097 588098 588099 588100 588794  589268 589754 589885 589886 590172 590404 590562 590776  591196 591197 591198 592080 592081 592526 592924 593080  593519 593520 593720 594204 594421 595195 595196 595418  595419 596020 597293 597294 597771 597905 597967 598903  599045 599466 599650 599903 601196 601745 601746 602260  603987 603988 603990 603991 604049 604500 604862 605617",
      "center_classification_date": "20170620",
      "distribution_pattern": "Worldwide Distribution - US (nationwide): including states of: AK, AL, AR, AZ, CA, CO, CT, DC,FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MN, MO, ME, MI, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY; and countries of: AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL, CANADA, CZECH REPUBLIC, EGYPT, FINLAND, FRANCE, GERMANY, GREECE, HONG KONG, IRELAND, ISRAEL, ITALY, LEBANON, NETHERLANDS, NORWAY, POLAND, RUSSIA, SAUDI ARABIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, TURKEY,and UK.",
      "state": "MN",
      "product_description": "Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822.  Sterilized using ethylene oxide, Rx Only.     The Venture catheter is indicated for directing, steering, controlling, and supporting a guidewire to access discrete regions of the coronary and peripheral vasculature. The OTW versions (Models 5821 and 5822) may also be used for manual delivery of saline solution or diagnostic contrast agents",
      "report_date": "20170628",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Vascular Solutions, Inc.",
      "recall_number": "Z-2224-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77202",
      "termination_date": "20191105",
      "more_code_info": "",
      "recall_initiation_date": "20170425",
      "postal_code": "55369-6032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}