{
  "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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  "results": [
    {
      "status": "Ongoing",
      "city": "Houston",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93115",
      "recalling_firm": "Alcon Research, LLC",
      "address_1": "9965 Buffalo Speedway",
      "address_2": "",
      "postal_code": "77054-1309",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US: VA OUS: None",
      "recall_number": "Z-0260-2024",
      "product_description": "Alcon Custom-Pak, Surgical Procedure Pack REF 14057-09, 45K W/DUOVISC CATARACT, N VIRGINIA EYE SURG CTR",
      "product_quantity": "120 packs",
      "reason_for_recall": "Custom surgical procedure packs contain latex gloves but are labeled as \"latex free\".",
      "recall_initiation_date": "20230907",
      "center_classification_date": "20231107",
      "report_date": "20231115",
      "code_info": "LOT # : 160NMU, UDI: (01)10380653302278",
      "more_code_info": ""
    }
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}