{
  "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": "The recalling firm received complaints related to leakage from the tubing near the white luer of the irrigation line for the INFINITI Ultrasound Packs.",
      "address_2": "",
      "product_quantity": "6597 packs",
      "code_info": "Lot numbers: 1623139H, 1623140H, 1623138H, 1623141H, 1623765H, 1623148H, 1623766H, 1623767H, 1623768H, 1623142H",
      "center_classification_date": "20160503",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "TX",
      "product_description": "INFINITI Ultrasound Pack. Catalog Numbers: 8065751716, 8065751717, 8065751718, 8065751720, 8065751721, 8065751723.  An ophthalmic microsurgical system indicated for phacoemulsification and removal of cataracts.",
      "report_date": "20160511",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Alcon Research, Ltd.",
      "recall_number": "Z-1597-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73767",
      "termination_date": "20170331",
      "more_code_info": "",
      "recall_initiation_date": "20141006",
      "postal_code": "76134-2099",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}