{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Fort Worth",
      "state": "TX",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71630",
      "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": "Distribution Japan,  No US distribution.",
      "recall_number": "Z-2323-2015",
      "product_description": "ReSTOR intraocular lens and ReSTOR Toric intraocular lens.    The Alcon AcrySof IQ ReSTOR and IQ ReSTOR Toric intraocular lenses are posterior chamber lenses intended as optical implants designed to replace the human crystalline lens in adult patients following cataract surgery. The lenses subject to this correction are manufactured specifically for Japan.",
      "product_quantity": "45,391",
      "reason_for_recall": "There are reports of post - operative inflammation and/or toxic anterior segment syndrome (TASS) after cataract surgery.",
      "recall_initiation_date": "20150415",
      "center_classification_date": "20150807",
      "termination_date": "20170630",
      "report_date": "20150819",
      "code_info": "Model Numbers: SN6AD1, SN6AD3, SV25T0, MN6AD1,SND1T3, SND1T4, SND1T5 and SND1T6 and all lot numbers."
    }
  ]
}