{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Houston",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79226",
      "recalling_firm": "Alcon Research, LTD.",
      "address_1": "9965 Buffalo Speedway",
      "address_2": "N/A",
      "postal_code": "77054-1309",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution :  Argentina  Australia  France  Italy  Mexico  Poland  Spain  Sweden  Russia  South Korea  Ukraine",
      "recall_number": "Z-0779-2018",
      "product_description": "Custom Pak¿  (Custom Pak in which Alcon 25+¿ TOTALPLUS¿ Vitrectomy Pak is a component.)    Includes all necessary items for a core vitrectomy procedure and connects to the CONSTELLATION Vision System.",
      "product_quantity": "52 units",
      "reason_for_recall": "Alcon is conducting this Voluntary Medical Device Recall for a specific lot (2060953H) of its 25+ TOTALPLUS Vitrectomy Pak due a potential that a 23GA ULTRAVIT probe may be included within the 25+ TOTALPLUS Vitrectomy Pak, instead of a 25+ ULTRAVIT probe.",
      "recall_initiation_date": "20180112",
      "center_classification_date": "20180228",
      "termination_date": "20220204",
      "report_date": "20180307",
      "code_info": "Lot 507492, 507664, 507539"
    }
  ]
}