{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Miami Lakes",
      "address_1": "14201 NW 60th Ave",
      "reason_for_recall": "Product was manufactured utilizing an expired inner body.",
      "address_2": "",
      "product_quantity": "21 units",
      "code_info": "Catalog Number: 4171460S; Lot Number: 82169860; Expiry Date: 10/31/2020",
      "center_classification_date": "20191030",
      "distribution_pattern": "US distribution to AL, AZ, FL, MN, and MO",
      "state": "FL",
      "product_description": "Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.",
      "report_date": "20191106",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cordis Corporation",
      "recall_number": "Z-0250-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83977",
      "termination_date": "20201214",
      "more_code_info": "",
      "recall_initiation_date": "20191004",
      "postal_code": "33014-2802",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}