{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Garland",
      "address_1": "2220 Merritt Dr",
      "reason_for_recall": "The adhesive used in the product could dislodge when objects are inserted through the valve which could pose an embolic risk to the patient.",
      "address_2": "",
      "product_quantity": "11,155 units in total",
      "code_info": "Catalog Numbers: NT-104-06, INT-104-07, INT-104-08, INT-104-09, INT-104-10, INT-104-11, INT-104-12, INT-104-17, INT-104-18, INT-104-19, INT-104-20, INT-104-21, INT-104-22, INT-104-23, INT-108-06, INT-108-07, INT-108-09, INT-108-10, INT-108-11, INT-108-12, INT-108-17, INT-108-18, INT-108-19, INT-108-20, INT-108-21, INT-108-22, INT-108-22, VTI-002-06, VTI-002-07, VTI-002-08, VTI-002-09, VTI-002-09, VTI-002-10, VTI-002-11, VTI-002-12, VTI-002-17, VTI-002-18, VTI-002-19, VTI-002-20, VTI-002-21, VTI-002-22, VTI-002-23, VTI-003-06, VTI-003-07, VTI-003-08, VTI-003-09, VTI-003-10, VTI-003-11, VTI-003-12, VTI-003-17, VTI-003-18, VTI-003-19, VTI-003-20, VTI-003-21, VTI-003-22, and VTI-003-23.",
      "center_classification_date": "20140904",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) Canada, Germany, the Netherlands, Ireland, Switzerland, France, Italy, and Greece.",
      "state": "TX",
      "product_description": "GALT VALVED TEARAWAY INTRODUCER SET  GALT VTI  RX ONLY UNITS 7  STERILE EO        Product Usage:  Used in percutaneous procedures to introduce catheters and other intravascular devices into the peripheral vasculature.",
      "report_date": "20140910",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Galt Medical Corporation",
      "recall_number": "Z-2588-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68939",
      "termination_date": "20160226",
      "more_code_info": "",
      "recall_initiation_date": "20140725",
      "postal_code": "75041-6137",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}