{
  "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": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93172",
      "recalling_firm": "Edwards Lifesciences, LLC",
      "address_1": "1 Edwards Way",
      "address_2": "",
      "postal_code": "92614-5688",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "OUS: Singapore, Taiwan, Canada",
      "recall_number": "Z-0238-2024",
      "product_description": "Fogarty Thru-Lumen Embolectomy Catheter, REF: 12TLW805F35",
      "product_quantity": "185",
      "reason_for_recall": "Inadvertent release of embolectomy catheters that may experience slower than normal balloon deflation (greater-than 15 seconds).",
      "recall_initiation_date": "20230907",
      "center_classification_date": "20231106",
      "report_date": "20231115",
      "code_info": "UDI-DI: 00690103043532, Lot: 64936927",
      "more_code_info": ""
    }
  ]
}