{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "North Brunswick",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97700",
      "recalling_firm": "LeMaitre Vascular, Inc.",
      "address_1": "206 N Center Dr",
      "address_2": "",
      "postal_code": "08902-4246",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to the state of: AR",
      "recall_number": "Z-0289-2026",
      "product_description": "Artegraft¿ Collagen Vascular Graft;  REF: AG1015;",
      "product_quantity": "1 unit",
      "reason_for_recall": "The device was incorrectly packed in the wrong size labeled outer packaging.",
      "recall_initiation_date": "20250925",
      "center_classification_date": "20251023",
      "report_date": "20251029",
      "code_info": "REF: AG1015; UDI-DI: 00316837000343; Lot/Serial Number: 23MM581-016;",
      "more_code_info": ""
    }
  ]
}