{
  "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-1443-2017",
      "product_description": "LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU)  REF# e2400-51",
      "product_quantity": "340",
      "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:  RED1752    2018-12  RED1758     2019-01  RED1772   2019-06"
    }
  ]
}