{
  "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": "74825",
      "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": "Letter",
      "distribution_pattern": "Burundi, China, Iran, South Korea, Taiwan, Thailand, USA. *** The recalled product is not sold in the USA or its territories.  However, donated units are in use by a reduced number of USA clients for Medical Missions outside the country.",
      "recall_number": "Z-2834-2016",
      "product_description": "LAUREATE World Phaco System",
      "product_quantity": "8,646 UNITS",
      "reason_for_recall": "Steps 16-25 are missing from the LAUREATE Multipak FMS Directions for Use (DFU)",
      "recall_initiation_date": "20160728",
      "center_classification_date": "20160915",
      "termination_date": "20170607",
      "report_date": "20160921",
      "code_info": "Lot Numbers: 1658863H, 1805033H, 1805034H, 1817516H, 1817517H, 1826141H, 1826142H, 1857622H, 1857623H, 1868399H, 1868400H",
      "more_code_info": ""
    }
  ]
}