{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Fort Worth",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72363",
      "recalling_firm": "Alcon Research, Ltd.",
      "address_1": "6201 South Fwy",
      "address_2": "N/A",
      "postal_code": "76134-2099",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Distributed in VT.",
      "recall_number": "Z-0195-2016",
      "product_description": "Custom Pak 9319-27.  Single-use medical devices and accessories designed by medical professionals for a specific ophthalmic surgical procedure.",
      "product_quantity": "5 units",
      "reason_for_recall": "The recalled lot of custom paks are labeled as latex free and contain latex gloves rather than the specified non-latex gloves.",
      "recall_initiation_date": "20150921",
      "center_classification_date": "20151030",
      "termination_date": "20160324",
      "report_date": "20151111",
      "code_info": "1792733H, 1783925H, 1785227H, 1786729H"
    }
  ]
}