{
  "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": "Clearwater",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67283",
      "recalling_firm": "Bausch & Lomb Surgical, Inc.",
      "address_1": "21 N Park Place Blvd",
      "address_2": "",
      "postal_code": "33759-3917",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and Internationally to: Great Britain, France, Spain, Portugal, Sweden, Russia and Guadeloupe.",
      "recall_number": "Z-1062-2014",
      "product_description": "Bausch & Lomb AKREOS AO Micro Incision Lens     The Akreos IOL intended for primary implantation in the capsular bag of the eye for the visual correction of aphakia secondary to the removal of a cataractous lens in adult patients.",
      "product_quantity": "336 IOLs (283 IOLs in the US, 53 IOLs outside the US)",
      "reason_for_recall": "Lens was manufactured with incorrect raw material.",
      "recall_initiation_date": "20131016",
      "center_classification_date": "20140220",
      "termination_date": "20140917",
      "report_date": "20140226",
      "code_info": "Model Numbers(s): AO60 and MI60L",
      "more_code_info": ""
    }
  ]
}