{
  "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": "Mountain View",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79386",
      "recalling_firm": "Iridex Corporation",
      "address_1": "1212 Terra Bella Ave",
      "address_2": "N/A",
      "postal_code": "94043-1824",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA Distribution and to the countries of :  China, Germany, Australia, Canada, Ireland, Lebanon, Japan, Israel and Qatar",
      "recall_number": "Z-1075-2018",
      "product_description": "Iridex TruFocus LIO Premiere\" Laser Indirect Ophthalmoscope ( LIO )       The LIO is a headmounted indirect ophthalmoscope which is used with a handheld lens to view and perform laser treatments on a patient s retina. It allows binocular visualization of the peripheral retina and can be used to evaluate and treat patients.",
      "product_quantity": "US - 58   OUS - 46",
      "reason_for_recall": "It was discovered that the laser energy was not going where intended to put it, resulting in focal cataracts and iris burns.",
      "recall_initiation_date": "20180227",
      "center_classification_date": "20180316",
      "termination_date": "20230922",
      "report_date": "20180328",
      "code_info": "Device Identity : 87300, 87301, 87302, 87303, 87304"
    }
  ]
}