{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Quincy",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79324",
      "recalling_firm": "Vascular Insights, LLC",
      "address_1": "1 Pine Hill Dr Ste 100",
      "address_2": "N/A",
      "postal_code": "02169-7485",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "U.S Nationwide in the states: AZ, CA, CT, FL, GA, IA, IL, IN, KS, KY, MA, MD, MO, NE, NJ, NY, OH, PA, SC, TN, TX, VA, WA",
      "recall_number": "Z-1146-2018",
      "product_description": "ClariVein IC infusion catheter, Model Number: 65-018-E4S    Product Usage:  The ClariVein IC infusion catheter is indicated for infusion of physician-specified agents into the peripheral vasculature.",
      "product_quantity": "928",
      "reason_for_recall": "Certain catheters could have a compromised catheter shaft due to a manufacturing defect which could result in some delamination of the catheter shaft including during introduction of the catheter into a vascular access introducer.",
      "recall_initiation_date": "20171109",
      "center_classification_date": "20180320",
      "termination_date": "20181218",
      "report_date": "20180328",
      "code_info": "Lot number: BM651403017I"
    }
  ]
}