{
  "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": "Santa Ana",
      "address_1": "1700 E Saint Andrew Pl",
      "reason_for_recall": "Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they were not being checked prior to release and this may result in the release of mislabeled IOLs.",
      "address_2": "",
      "product_quantity": "1 unit",
      "code_info": "Serial No.  5050941602",
      "center_classification_date": "20160921",
      "distribution_pattern": "Worldwide Distribution - US nationwide, PR, and Internationally to Canada, Latin America, Europe, Africa, Middle East, and Asia Pacific.",
      "state": "CA",
      "product_description": "SENSAR 1-Piece IOL, Model No. AAB00  The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag.",
      "report_date": "20160928",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Abbott Medical Optics Inc. (AMO)",
      "recall_number": "Z-2860-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75051",
      "termination_date": "20161223",
      "more_code_info": "",
      "recall_initiation_date": "20160826",
      "postal_code": "92705-4933",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}