{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Miami Lakes",
      "state": "FL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93174",
      "recalling_firm": "Cordis US Corp",
      "address_1": "14201 Nw 60th Ave",
      "address_2": "",
      "postal_code": "33014-2802",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Distribution to: OK",
      "recall_number": "Z-0286-2024",
      "product_description": "Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter",
      "product_quantity": "30 devices",
      "reason_for_recall": "Non-sterile product labeled as sterile was distributed.",
      "recall_initiation_date": "20230926",
      "center_classification_date": "20231109",
      "report_date": "20231115",
      "code_info": "UDI/DI 10705032025935, Lot Number 18223410",
      "more_code_info": ""
    }
  ]
}