{
  "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": {
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    {
      "status": "Ongoing",
      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93010",
      "recalling_firm": "Alcon Research, LLC",
      "address_1": "15800 Alton Pkwy",
      "address_2": "N/A",
      "postal_code": "92618-3818",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "US: GA, IL, PR",
      "recall_number": "Z-0099-2024",
      "product_description": "Constellation Vision System, REF: 8065751150",
      "product_quantity": "3",
      "reason_for_recall": "Ophthalmic microsurgical vision systems have a new Printed Circuit Board (PCB) design that could lead to higher voltage to a PCB component, that could cause component failure and loss of pressure control for the use of cutters, scissors, and forceps, which could lead to an increased risk of microbial infection, tissue damage and progressive visual impairment.",
      "recall_initiation_date": "20230818",
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      "code_info": "UDI-DI: 00380657511501, Serial Numbers: 1403028701X, 1202865201X, 0802983301X"
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}