{
  "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": [
    {
      "status": "Terminated",
      "city": "Burlington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76476",
      "recalling_firm": "LeMaitre Vascular, Inc.",
      "address_1": "63 2nd Ave",
      "address_2": "N/A",
      "postal_code": "01803-4413",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution.  US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore,   SPAIN, SWITZERLAND, UAE, and UK",
      "recall_number": "Z-1447-2017",
      "product_description": "LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter (paper IFU)  REF#  2401-50",
      "product_quantity": "403",
      "reason_for_recall": "The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch",
      "recall_initiation_date": "20170207",
      "center_classification_date": "20170313",
      "termination_date": "20190920",
      "report_date": "20170322",
      "code_info": "Lot Number/Exp. Date:  RST2404                 2018-012  RST2416                  2019-02  RST2424                  2019-03  RST2426                  2019-03  RST2442                  2019-07"
    }
  ]
}