{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Santa Ana",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64015",
      "recalling_firm": "Abbott Medical Optics Inc (AMO)",
      "address_1": "1700 E Saint Andrew Pl",
      "address_2": "N/A",
      "postal_code": "92705-4933",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide including the state of OH and the countries of:  Germany, Switzerland, Sweden, Italy, China, France, Singapore, UK, Croatia, Hungary, Turkey and Brazil.",
      "recall_number": "Z-0929-2013",
      "product_description": "AMO Sensar Intraocular Lenses (IOLs), Model AR40e,   Sensar Foldable IOL with OptiEdge     Product Usage:  These are ultraviolet-absorbing posterior chamber intraocular lenses for use after cataract extraction.",
      "product_quantity": "155 units",
      "reason_for_recall": "Two production orders of these IOLs that contain mislabeled IOLs.",
      "recall_initiation_date": "20121220",
      "center_classification_date": "20130309",
      "termination_date": "20140108",
      "report_date": "20130320",
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