{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Miami Lakes",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84680",
      "recalling_firm": "Cordis Corporation",
      "address_1": "14201 NW 60th Ave",
      "address_2": "",
      "postal_code": "33014-2802",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US and UK",
      "recall_number": "Z-1477-2020",
      "product_description": "Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S",
      "product_quantity": "89 units",
      "reason_for_recall": "Cordis is recalling one (1) lot of POWERFLEX P3 PTA Dilatation Catheter due to the potential for body/shaft voids in the proximal seal area.",
      "recall_initiation_date": "20200108",
      "center_classification_date": "20200312",
      "termination_date": "20230113",
      "report_date": "20200318",
      "code_info": "Lot 82155955, Use by date 2021-06-30",
      "more_code_info": ""
    }
  ]
}