{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94119",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, Ireland, United Kingdom, and Hong Kong.",
      "recall_number": "Z-1524-2024",
      "product_description": "Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers:  US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, and US-AS46-230002 CV Specialty Brochure   US version which affect:  Vascular Probe, Item Numbers: a) 7081015, b) 7081015ES, c) 7081520, d) 7081520ES, e) 7082025, f) 7082025ES, g) 7151015, h) 7151015ES, i) 7151520, j) 7151520ES, k) 7152025, l) 7152025ES, m) 7451015, n) 7451015ES, o) 7451520, p) 7451520ES, q) 7452025, r) 7452025ES",
      "product_quantity": "82020 units",
      "reason_for_recall": "The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe Intravascular Probe contain inaccurate content that does not align with the products\u0019 Instructions for Use (IFU).",
      "recall_initiation_date": "20240222",
      "center_classification_date": "20240412",
      "report_date": "20240424",
      "code_info": "Cardiovascular Specialty marketing brochures: Reference numbers:  US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, and US-AS46-230002 CV Specialty Brochure   US version;  Flo-Thru Intraluminal Shunt:  ALL SERIAL NUMBERS:  a) 7081015, UDI/DI00085412532554;  b) 7081015ES, UDI/DI00085412532646;  c) 7081520, UDI/DI00085412532561;  d) 7081520ES, UDI/DI00085412532653;  e) 7082025, UDI/DI00085412532578;  f) 7082025ES, UDI/DI00085412532660;  g) 7151015, UDI/DI00085412532585;  h) 7151015ES, UDI/DI00085412532677;  i) 7151520, UDI/DI00085412531908;  j) 7151520ES, UDI/DI00085412531915;  k) 7152025, UDI/DI00085412531922;  l) 7152025ES, UDI/DI00085412531939;  m) 7451015, UDI/DI00085412531946;  n) 7451015ES, UDI/DI00085412531953;  o) 7451520, UDI/DI00085412531960;  p) 7451520ES, UDI/DI00085412531977;  q) 7452025, UDI/DI00085412531984;  r) 7452025ES, UDI/DI00085412531991",
      "more_code_info": ""
    }
  ]
}