{
  "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,
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  },
  "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": "84 units",
      "code_info": "Serial No.  5626941507  5626961507  5626981507  5627001507  2003061505  2004131506  2015871503  3848581509  5626621507  5626641507  5626651507  5626661507  5626671507  5626681507  5626691507  5626701507  5626711507  5626721507  5626731507  5626741507  5626751507  5626761507  5626771507  5626791507  5626801507  5626811507  5626821507  5626831507  5626841507  5626851507  5626861507  5626871507  5626881507  5626891507  5626901507  5626911507  5626921507  5626931507  5626951507  5626971507  5627011507  5627021507  5627031507  5627041507  5627051507  5627061507  5627071507  5627081507  5627091507  5627101507  5627111507  5627121507  5627131507  5627141507  5627151507  5627161507  5627171507  5627181507  5627191507  5627201507  5627211507  5627221507",
      "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 Foldable IOL with OptiEdge Design, Model No. AR40e  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-2855-2016",
      "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"
    }
  ]
}