{
  "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": "2026-10-14",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Burlington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99836",
      "recalling_firm": "LeMaitre Vascular, Inc.",
      "address_1": "32 3rd Ave",
      "address_2": "N/A",
      "postal_code": "01803-4414",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, FL, GA, KY, LA, NJ, OH, PA, SC.",
      "recall_number": "Z-0117-2027",
      "product_description": "TufTex¿ Over-the-Wire Embolectomy Catheter;  Catalog Number: E1651-88;",
      "product_quantity": "54",
      "reason_for_recall": "Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing.",
      "recall_initiation_date": "20260828",
      "center_classification_date": "20261007",
      "report_date": "20261014",
      "code_info": "Catalog Number: E1651-88; UDI-DI: 00840663100866; Lot Number: XOT00002181;"
    }
  ]
}