{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91318",
      "recalling_firm": "Covidien, LLC",
      "address_1": "161 Cheshire Ln N Ste 100",
      "address_2": "",
      "postal_code": "55441-5433",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "Foreign Distribution: Hong Kong",
      "recall_number": "Z-0955-2023",
      "product_description": "COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1",
      "product_quantity": "21 units",
      "reason_for_recall": "The product is labeled with the incorrect expiration date.",
      "recall_initiation_date": "20221123",
      "center_classification_date": "20230112",
      "report_date": "20230118",
      "code_info": "UDI/DI (GTIN): 10884521825765, Lot Number: 520200",
      "more_code_info": ""
    }
  ]
}