{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Fort Worth",
      "address_1": "6201 South Fwy",
      "reason_for_recall": "The intraocular lens could become lodged within the cartridge",
      "address_2": "",
      "product_quantity": "1,130 units",
      "code_info": "Alcon Monarch II C Cartridge Model 8065977762, Lot Number 32395407, Manufacture Date 8/13/2015",
      "center_classification_date": "20170109",
      "distribution_pattern": "Distributed to Mexico only",
      "state": "TX",
      "product_description": "Alcon Monarch III (1) \"C\" Cartridge  The device is used for implanting AcrySof intraocular lenses in the eye following cataract removal",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Alcon Research, Ltd.",
      "recall_number": "Z-0978-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75049",
      "termination_date": "20170210",
      "more_code_info": "",
      "recall_initiation_date": "20160905",
      "postal_code": "76134-2099",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
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}