{
  "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-1448-2017",
      "product_description": "LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter with Introducer (eIFU)  REF#  e2401-51",
      "product_quantity": "2065",
      "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:  RST2403    2018-12  RST2409    2019-01  RST2410    2019-01  RST2427    2019-03  RST2434   2019-05  RST2439   2019-06  RST2444   2019-07"
    }
  ]
}