{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Fort Worth",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97415",
      "recalling_firm": "Alcon Research LLC",
      "address_1": "6201 South Fwy",
      "address_2": "N/A",
      "postal_code": "76134-2099",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution: US (nationwide): AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC,SD,TN, TX, VA, WA, WI,  and WV; and OUS (foreign) to countries of: Argentina, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belgium, Brazil,  Brunei, Canada, Chile, China, Colombia, Croatia, Czechia, Denmark, Finland, France, Germany, Greece, Guadeloupe, Hong Kong, Hungary, Iceland, India, Ireland, Israel, Italy, Japan, Korea, Kosovo, Luxembourg, Malaysia, Mexico, Moldova, Montenegro, Morocco, Netherlands, New Zealand, Pakistan, Peru, Philippines, Poland, Portugal, Qatar, Reunion, Russian Federation, Saudi Arabia, Serbia, Slovakia, South Africa, Spain, Sri Lanka, Sweden, Switzerland, Taiwan, Turkey, United Arab Emirates, and United Kingdom,",
      "recall_number": "Z-0307-2026",
      "product_description": "Brand Name: Alcon Laboratories, Inc.  Product Name: Accessory devices for Unity and Constellation surgical consoles  Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List'  8065000252\tUNITY 27 GA CHANDELIER  8065000253\tUNITY 27+DS WIDE ANGLE LIGHT PROBE    Software Version: N/A  Product Description: These products are standalone accessory devices meant for vitrectomy surgical procedures. They interface with a corresponding Alcon surgical console.  Component: N/A",
      "product_quantity": "330",
      "reason_for_recall": "Due to incomplete seals in the pouch which provide the sterile barrier.",
      "recall_initiation_date": "20250805",
      "center_classification_date": "20251024",
      "report_date": "20251105",
      "code_info": "Catalog Number: 8065000252 UDI-DI code: 00380650002525 Lot/Batch Numbers: 17CMKR 17D417  Catalog Number: 8065000253 UDI-DI code: 00380650002532 Lot/Batch Number: 17CDMX"
    }
  ]
}