{
  "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": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72434",
      "recalling_firm": "Tekia,  Inc.",
      "address_1": "17 Hammond Ste 414",
      "address_2": "N/A",
      "postal_code": "92618-1635",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Internationally to Vietnam.",
      "recall_number": "Z-0237-2016",
      "product_description": "TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811",
      "product_quantity": "50 units",
      "reason_for_recall": "Tekia is recalling the Single Piece Hydrophillic Acrylic Intraocular Lenses (IOLs) because they may be labeled with the incorrect diopter power.",
      "recall_initiation_date": "20150929",
      "center_classification_date": "20151106",
      "termination_date": "20151203",
      "report_date": "20151118",
      "code_info": "SN: U07310001 thru U07310040 , 07310050 thru U07310059"
    }
  ]
}