{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "West Henrietta",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91793",
      "recalling_firm": "CooperVision, Inc.",
      "address_1": "180 Thruway Park Dr",
      "address_2": "N/A",
      "postal_code": "14586-9798",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of FL, IL, NY, UT, and WI. The country of Canada.",
      "recall_number": "Z-1282-2023",
      "product_description": "Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90",
      "product_quantity": "3150",
      "reason_for_recall": "The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.",
      "recall_initiation_date": "20230214",
      "center_classification_date": "20230323",
      "report_date": "20230329",
      "code_info": "Lot Number W0124677"
    }
  ]
}