{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Somerset",
      "address_1": "2101 Cottontail Ln",
      "reason_for_recall": "Two lots of product were released for distribution prior to the completion of all required validation and lot acceptance activities. Although sterile, products from these lots may not function as intended and therefore should not be used.",
      "address_2": "",
      "product_quantity": "240",
      "code_info": "5980075, 5980077",
      "center_classification_date": "20180629",
      "distribution_pattern": "Distributed to accounts in AL, CA, FL, IA, IN, MI, MO, NC, NY, SD, TN, and TX.",
      "state": "NJ",
      "product_description": "Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135",
      "report_date": "20180711",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Terumo Medical Corp",
      "recall_number": "Z-2337-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80242",
      "termination_date": "20190419",
      "more_code_info": "",
      "recall_initiation_date": "20180409",
      "postal_code": "08873-1277",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}