{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Fort Worth",
      "address_1": "Aspex Facility",
      "reason_for_recall": "Incorrect IOL diopter",
      "address_2": "6201 South Fwy",
      "product_quantity": "84 units",
      "code_info": "Lot number 12726594; Model Number: AU00T0V205; UDI # 038065GMN000065H7; 0380652394772(17)220630(21)12726594000(30)1",
      "center_classification_date": "20200605",
      "distribution_pattern": "US Nationwide distribution including in the states of TX, PA, CT, IA, MI, NE.",
      "state": "TX",
      "product_description": "Acrysof, IQ IOL w/UltraSert System, AcrySof IQ ASPHERIC IOL, 20.5 D, SP ACRYLIC FOLDABLE LENS, w/UltraSert DELIVERY SYSTEM, UV w/BLUE LIGHT FILTER. 13.0mm. LENGTH, 6.0mm ANTERIOR ASYMMETRIC BICONVEX OPTIC, PLANAR HAPTICS.",
      "report_date": "20200617",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Alcon Research LLC",
      "recall_number": "Z-2287-2020",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "85563",
      "termination_date": "20210205",
      "recall_initiation_date": "20200417",
      "postal_code": "76134-2099",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}