{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Fort Worth",
      "address_1": "6201 South Fwy",
      "reason_for_recall": "There was a potential that a 25-gauge infusion cannula may be included within the procedure pak instead of a 20-gauge infusion cannula.",
      "address_2": "Aspex Facility",
      "product_quantity": "102 packs",
      "code_info": "Lot #2128524H",
      "center_classification_date": "20200423",
      "distribution_pattern": "There was no domestic distribution.  Foreign distribution was made to Germany, Iraq, Israel, Italy, and Moldova.",
      "state": "TX",
      "product_description": "Alcon Constellation Vision System 20 GA TOTALPLUS Combined Procedure Pak, Product #8065751079, Sterile.  The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.",
      "report_date": "20200429",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Alcon Research LLC",
      "recall_number": "Z-1794-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "85198",
      "termination_date": "20200424",
      "recall_initiation_date": "20180725",
      "postal_code": "76134-2099",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}