{
  "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": "Houston",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77965",
      "recalling_firm": "Alcon Research, LTD.",
      "address_1": "9965 Buffalo Speedway",
      "address_2": "N/A",
      "postal_code": "77054-1309",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "States in the US - WI, NY, MO",
      "recall_number": "Z-0053-2018",
      "product_description": "Alcon Custom Pak",
      "product_quantity": "33 units",
      "reason_for_recall": "Alcon is initiating a medical device recall, after receiving notification from a supplier of a recall for x-ray detectable sponges.  The one product referenced in the supplier recall notification, is used within Alcon Custom Paks.",
      "recall_initiation_date": "20170808",
      "center_classification_date": "20171027",
      "termination_date": "20190805",
      "report_date": "20171108",
      "code_info": "2033459H, 2034186H, 2034491H"
    }
  ]
}