{
  "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": "2026-04-22",
    "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": "64704",
      "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-USA (nationwide) and the countries of  Canada, EU, and Asia.",
      "recall_number": "Z-1054-2013",
      "product_description": "LeMaitre Stent Guide: 1102-00 (100 strips); 1102-50 (50 strips); 1102-20 (20 strips).    Intended to be placed on the skin to assist during imaging procedures.",
      "product_quantity": "6970",
      "reason_for_recall": "Devices were not sealed correctly during the manufacturing process, and the sterility of these products have been compromised.",
      "recall_initiation_date": "20130318",
      "center_classification_date": "20130404",
      "termination_date": "20141203",
      "report_date": "20130410",
      "code_info": "LSG1130, exp. 2017-04; LSG1132, exp. 2017-11"
    }
  ]
}