{
  "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": [
    {
      "status": "Terminated",
      "city": "Miami Lakes",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88348",
      "recalling_firm": "Cordis Corporation",
      "address_1": "14201 NW 60th Ave",
      "address_2": "N/A",
      "postal_code": "33014-2802",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of CA, OH, and the countries of Switzerland, Portugal, and Poland.",
      "recall_number": "Z-2235-2021",
      "product_description": "Cordis SABER PTA Balloon Dilation Catheter, 4F, REF 48004010X",
      "product_quantity": "8 units",
      "reason_for_recall": "The balloon protective sheath may potentially be contaminated with a foreign material left over from the manufacturing process. The contaminant may transfer over from the sheath to the balloon.",
      "recall_initiation_date": "20210719",
      "center_classification_date": "20210809",
      "termination_date": "20230216",
      "report_date": "20210818",
      "code_info": "Lot/Batch number 82219442"
    }
  ]
}