{
  "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": "2026-09-05",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "179522",
      "product_res_number": "Z-1821-2020",
      "event_date_initiated": "2018-08-01",
      "event_date_created": "2020-04-29",
      "recall_status": "Completed",
      "res_event_number": "84839",
      "product_code": "LPM",
      "pma_numbers": [
        "P010019"
      ],
      "product_description": "Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.",
      "code_info": "Lot numbers 31202568; 31255298; 31257909; 31229117; 31252252.",
      "firm_fei_number": "1000122287",
      "recalling_firm": "Allied Vision Group Inc",
      "address_1": "5350 Nw 35th Ave",
      "city": "Fort Lauderdale",
      "state": "FL",
      "postal_code": "33309-6314",
      "additional_info_contact": "Robert Lesica\n954-730-9244",
      "reason_for_recall": "Potentially counterfeit products in/and counterfeit packaging were imported to the U.S.",
      "root_cause_description": "Counterfeit",
      "action": "The firm initiated the recall by email on August 01, 2018 and followed with a second email on August 03, 2018.  The email explained that the product was potentially non-genuine and offered a full refund or exchange of the product.",
      "product_quantity": "655 boxes with 6 units per box.  total 3930",
      "distribution_pattern": "Worldwide and US Nationwide",
      "openfda": {
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        "device_name": "Lenses, Soft Contact, Extended Wear",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.5925",
        "device_class": "3"
      }
    }
  ]
}