{
  "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-1450-2017",
      "product_description": "LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)  REF#  e2401-52",
      "product_quantity": "4673",
      "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:  RST2391    2018-09  RST2394    2018-09  RST2395    2018-09  RST2406    2018-12  RST2407    2018-12  RST2414    2019-02  RST2415    2019-02  RST2421    2019-03  RST2422    2019-03  RST2429    2019-04  RST2430    2019-04  RST2435    2019-05  RST2445    2019-07  RST2446    2019-07  RST2451    2019-08"
    }
  ]
}