{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Galway",
      "state": "N/A",
      "country": "Ireland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92608",
      "recalling_firm": "Creganna Medical Devices",
      "address_1": "Parkmore House",
      "address_2": "Mweeloon",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of AZ.",
      "recall_number": "Z-2249-2023",
      "product_description": "Gore Tips Set Device, Catalog Number TSET1016, percutaneous liver access",
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      "reason_for_recall": "Three lots of product may be labeled with an incorrect expiration day",
      "recall_initiation_date": "20230622",
      "center_classification_date": "20230728",
      "report_date": "20230809",
      "code_info": "UDI/DI 05391526210000, Lot Numbers:  1V00099635, 1V00166928, 1V00199622"
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}