{
  "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": "2026-08-22",
    "results": {
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      "cfres_id": "37157",
      "product_res_number": "Z-0558-05",
      "event_date_initiated": "2005-02-07",
      "event_date_posted": "2005-02-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-07-25",
      "res_event_number": "31108",
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      "code_info": "Lot Numbers: SLC1201, SLC1213",
      "firm_fei_number": "1220948",
      "recalling_firm": "Lemaitre Vascular, Inc.",
      "address_1": "63 2nd Ave",
      "city": "Burlington",
      "state": "MA",
      "postal_code": "01803-4413",
      "additional_info_contact": "Trent Kamke\n781-221-2266 Ext. 105",
      "reason_for_recall": "Product sterility maybe compromised due to defective packaging",
      "root_cause_description": "Other",
      "action": "LaMaitre notified consignees by lettter advising users to check inventory and return defective product.",
      "product_quantity": "692 units",
      "distribution_pattern": "AL, CA, FL, IN, MD, MI,NY, TN, \n\nFOREIGN: Germany",
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        "device_name": "Catheter, Embolectomy",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.5150",
        "device_class": "2"
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