{
  "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": [
    {
      "country": "United States",
      "city": "Juana Diaz",
      "address_1": "#500  Road 584",
      "reason_for_recall": "The lenses exceeded the acceptance limit for silicone oil residual.",
      "address_2": "Amuelas Industrial Park",
      "product_quantity": "246",
      "code_info": "10447500016006, 10519550007006, 10537500016014",
      "center_classification_date": "20130103",
      "distribution_pattern": "US Nationwide, including Puerto Rico, and Canada.",
      "state": "PR",
      "product_description": "AVAIRA (enfilcon A) Soft (Hydrophilic) Daily Wear Toric Contact Lenses",
      "report_date": "20130109",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cooper Vision Caribbean Corp.",
      "recall_number": "Z-0631-2013",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "63719",
      "termination_date": "20140509",
      "recall_initiation_date": "20121109",
      "postal_code": "00795",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}