{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Sarasota",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87421",
      "recalling_firm": "Clerio Vision",
      "address_1": "7575 Commerce Ct",
      "address_2": "N/A",
      "postal_code": "34243-3218",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of  Illinois and Missouri, and the countries of Denmark, Germany, The Netherlands, Switzerland.",
      "recall_number": "Z-1352-2021",
      "product_description": "EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for daily wear - Product Usage: indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that are myopic or hyperopic. The lens may be worn by persons who exhibit astigmatism of 0.75 Diopters or less that does not interfere with visual acuity.",
      "product_quantity": "153 lenses",
      "reason_for_recall": "Contact lenses may be mislabeled with the incorrect lens power.",
      "recall_initiation_date": "20210216",
      "center_classification_date": "20210405",
      "termination_date": "20230705",
      "report_date": "20210414",
      "code_info": "Lot Number: 0114511565, UPC Code: 675506700657 (6 pack), 675506668650 (individual)"
    }
  ]
}